Canonical Allele Identifier: CA467852744
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136131101C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255714C>A , CM000671.2:g.133255714C>A GRCh38
NC_000009.11:g.136131101C>A , CM000671.1:g.136131101C>A GRCh37
NC_000009.10:g.135120922C>A NCBI36
NG_006669.1:g.21954G>T
NG_006669.2:g.24502G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1046G>T
ENST00000647353.1:n.54-4562G>T
ENST00000679909.1:c.28+19448G>T ENSP00000506089.1:n.28+19448G>T
ENST00000453660.3:n.1028G>T
ENST00000538324.2:c.1014G>T ENSP00000483018.1:p.Leu338=
ENST00000611156.4:c.1014G>T ENSP00000483265.1:p.Leu338=
NM_020469.2:c.1017G>T NP_065202.2:p.Leu339=
NM_020469.3:c.1017G>T NP_065202.2:p.Leu339=