Canonical Allele Identifier: CA375685153

Gene: ABO

Linked Data

• dbSNP Id: rs1362603574
• gnomAD v2: 9-136131330-A-G
• gnomAD v4: 9-133255943-A-G
• MyVariant Identifiers: chr9:g.136131330A>G (hg19) ; chr9:g.133255943A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255943A>G , CM000671.2:g.133255943A>G	GRCh38
NC_000009.11:g.136131330A>G , CM000671.1:g.136131330A>G	GRCh37
NC_000009.10:g.135121151A>G	NCBI36
NG_006669.1:g.21725T>C
NG_006669.2:g.24273T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.817T>C
ENST00000647353.1:n.54-4791T>C
ENST00000679909.1:c.28+19219T>C	ENSP00000506089.1:n.28+19219T>C
ENST00000453660.3:n.799T>C
ENST00000538324.2:c.785T>C	ENSP00000483018.1:p.Phe262Ser
ENST00000611156.4:c.785T>C	ENSP00000483265.1:p.Phe262Ser
NM_020469.2:c.788T>C	NP_065202.2:p.Phe263Ser
NM_020469.3:c.788T>C	NP_065202.2:p.Phe263Ser