Canonical Allele Identifier: CA397317782

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4933230G>T , CM000679.2:g.4933230G>T GRCh38
NC_000017.10:g.4836525G>T , CM000679.1:g.4836525G>T GRCh37
NC_000017.9:g.4777305G>T NCBI36
NG_008767.2:g.5936G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000329125.6:c.626G>T (GP1BA) MANE Select ENSP00000329380.5:p.Gly209Val
ENST00000649830.1:c.-888+1112C>A (CHRNE) ENSP00000496907.1:n.-888+1112C>A
ENST00000329125.5:c.626G>T (GP1BA) ENSP00000329380.5:p.Gly209Val
ENST00000611961.1:c.626G>T (GP1BA) ENSP00000484439.1:p.Gly209Val
NM_000173.6:c.626G>T (GP1BA) NP_000164.5:p.Gly209Val
NM_000173.7:c.626G>T (GP1BA) MANE Select NP_000164.5:p.Gly209Val