Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 2:26461756 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM024260

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 11 HGVS names - click the plus to show

2:g.26461756G>C
ENST00000403946.4:c.5473C>G
ENSP00000385255.3:p.Pro1825Ala
ENST00000338581.7:c.3172C>G
ENSP00000345137.6:p.Pro1058Ala
ENST00000272371.3:c.5473C>G
ENSP00000272371.2:p.Pro1825Ala
ENST00000339598.4:c.3172C>G
ENSP00000344521.3:p.Pro1058Ala
ENST00000402415.4:c.3403C>G
ENSP00000383906.3:p.Pro1135Ala

Variation displays