Canonical Allele Identifier: CA375685100

Gene: ABO

Linked Data

• gnomAD v4: 9-133255935-G-C
• MyVariant Identifiers: chr9:g.136131322G>C (hg19) ; chr9:g.133255935G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255935G>C , CM000671.2:g.133255935G>C	GRCh38
NC_000009.11:g.136131322G>C , CM000671.1:g.136131322G>C	GRCh37
NC_000009.10:g.135121143G>C	NCBI36
NG_006669.1:g.21733C>G
NG_006669.2:g.24281C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.825C>G
ENST00000647353.1:n.54-4783C>G
ENST00000679909.1:c.28+19227C>G	ENSP00000506089.1:n.28+19227C>G
ENST00000453660.3:n.807C>G
ENST00000538324.2:c.793C>G	ENSP00000483018.1:p.Leu265Val
ENST00000611156.4:c.793C>G	ENSP00000483265.1:p.Leu265Val
NM_020469.2:c.796C>G	NP_065202.2:p.Leu266Val
NM_020469.3:c.796C>G	NP_065202.2:p.Leu266Val