Canonical Allele Identifier: CA467853079

Gene: ABO

Linked Data

• dbSNP Id: rs1834567028
• gnomAD v4: 9-133255900-C-T
• MyVariant Identifiers: chr9:g.136131287C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255900C>T , CM000671.2:g.133255900C>T	GRCh38
NC_000009.11:g.136131287C>T , CM000671.1:g.136131287C>T	GRCh37
NC_000009.10:g.135121108C>T	NCBI36
NG_006669.1:g.21768G>A
NG_006669.2:g.24316G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.860G>A
ENST00000647353.1:n.54-4748G>A
ENST00000679909.1:c.28+19262G>A	ENSP00000506089.1:n.28+19262G>A
ENST00000453660.3:n.842G>A
ENST00000538324.2:c.828G>A	ENSP00000483018.1:p.Val276=
ENST00000611156.4:c.828G>A	ENSP00000483265.1:p.Val276=
NM_020469.2:c.831G>A	NP_065202.2:p.Val277=
NM_020469.3:c.831G>A	NP_065202.2:p.Val277=