Canonical Allele Identifier: CA467852807
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136131374G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255987G>T , CM000671.2:g.133255987G>T GRCh38
NC_000009.11:g.136131374G>T , CM000671.1:g.136131374G>T GRCh37
NC_000009.10:g.135121195G>T NCBI36
NG_006669.1:g.21681C>A
NG_006669.2:g.24229C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.773C>A
ENST00000647353.1:n.54-4835C>A
ENST00000679909.1:c.28+19175C>A ENSP00000506089.1:n.28+19175C>A
ENST00000453660.3:n.755C>A
ENST00000538324.2:c.741C>A ENSP00000483018.1:p.Arg247=
ENST00000611156.4:c.741C>A ENSP00000483265.1:p.Arg247=
NM_020469.2:c.744C>A NP_065202.2:p.Arg248=
NM_020469.3:c.744C>A NP_065202.2:p.Arg248=