Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 11:17387935 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM050651, CM050650

Most severe consequence
Evidence status

Clinical significance

This variation has 11 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

Variant allele T
11:g.17387935C>T
ENST00000526912.1:c.-17+83G>A
ENST00000528992.1:c.174G>A
ENSP00000436479.1:p.Gly59Ser
ENST00000528731.1:c.-16-89G>A
ENST00000339994.4:c.157G>A
ENSP00000345708.4:p.Gly53Ser

Variant allele G
11:g.17387935C>G
ENST00000526912.1:c.-17+83G>C
ENST00000528992.1:c.174G>C
ENSP00000436479.1:p.Gly59Arg
ENST00000528731.1:c.-16-89G>C
ENST00000339994.4:c.157G>C
ENSP00000345708.4:p.Gly53Arg

Variation displays