Canonical Allele Identifier: CA375683108

Gene: ABO

Linked Data

• gnomAD v4: 9-133255671-G-A
• MyVariant Identifiers: chr9:g.136131058G>A (hg19) ; chr9:g.133255671G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255671G>A , CM000671.2:g.133255671G>A	GRCh38
NC_000009.11:g.136131058G>A , CM000671.1:g.136131058G>A	GRCh37
NC_000009.10:g.135120879G>A	NCBI36
NG_006669.1:g.21997C>T
NG_006669.2:g.24545C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1089C>T
ENST00000647353.1:n.54-4519C>T
ENST00000679909.1:c.28+19491C>T	ENSP00000506089.1:n.28+19491C>T
ENST00000453660.3:n.1071C>T
ENST00000538324.2:c.1054-1C>T	ENSP00000483018.1:n.1054-1C>T
ENST00000611156.4:c.1057C>T	ENSP00000483265.1:p.Pro353Ser
NM_020469.2:c.1060C>T	NP_065202.2:p.Pro354Ser
NM_020469.3:c.1060C>T	NP_065202.2:p.Pro354Ser