Canonical Allele Identifier: CA200764781

Gene: ABO

Linked Data

• dbSNP Id: rs62641786
• gnomAD v2: 9-136130677-T-C
• gnomAD v3: 9-133255290-T-C
• gnomAD v4: 9-133255290-T-C
• MyVariant Identifiers: chr9:g.136130677T>C (hg19) ; chr9:g.133255290T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133255290T>C , CM000671.2:g.133255290T>C	GRCh38
NC_000009.11:g.136130677T>C , CM000671.1:g.136130677T>C	GRCh37
NC_000009.10:g.135120498T>C	NCBI36
NG_006669.1:g.22378A>G
NG_006669.2:g.24926A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.1470A>G
ENST00000647353.1:n.54-4138A>G
ENST00000679909.1:c.28+19872A>G	ENSP00000506089.1:n.28+19872A>G
ENST00000453660.3:n.1452A>G
ENST00000611156.4:c.*376A>G	ENSP00000483265.1:n.*376A>G
NM_020469.2:c.*376A>G	NP_065202.2:n.*376A>G
NM_020469.3:c.*376A>G	NP_065202.2:n.*376A>G