Canonical Allele Identifier: CA397317632

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933206A>C , CM000679.2:g.4933206A>C GRCh38
NC_000017.10:g.4836501A>C , CM000679.1:g.4836501A>C GRCh37
NC_000017.9:g.4777281A>C NCBI36
NG_008767.2:g.5912A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.602A>C (GP1BA) MANE Select ENSP00000329380.5:p.Tyr201Ser
ENST00000649830.1:c.-888+1136T>G (CHRNE) ENSP00000496907.1:n.-888+1136T>G
ENST00000329125.5:c.602A>C (GP1BA) ENSP00000329380.5:p.Tyr201Ser
ENST00000611961.1:c.602A>C (GP1BA) ENSP00000484439.1:p.Tyr201Ser
NM_000173.6:c.602A>C (GP1BA) NP_000164.5:p.Tyr201Ser
NM_000173.7:c.602A>C (GP1BA) MANE Select NP_000164.5:p.Tyr201Ser