Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 11:17474961 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM072816

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 9 HGVS names - click the plus to show

11:g.17474961T>C
ENST00000389817.5:c.215A>G
ENSP00000374467.3:p.Asn72Ser
ENST00000527905.3:c.215A>G
ENSP00000431653.1:p.Asn72Ser
ENST00000532728.3:n.246A>G
ENST00000302539.6:c.215A>G
ENSP00000303960.4:p.Asn72Ser
ENST00000612903.1:c.148+1668A>G

Variation displays