Canonical Allele Identifier: CA2692330850

Gene: ABO

Linked Data

• gnomAD v4: 9-133258199-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258199T>C , CM000671.2:g.133258199T>C	GRCh38
NC_000009.11:g.136133590T>C , CM000671.1:g.136133590T>C	GRCh37
NC_000009.10:g.135123411T>C	NCBI36
NG_006669.1:g.19464A>G
NG_006669.2:g.22016A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-67A>G
ENST00000647353.1:n.54-7047A>G
ENST00000651471.1:n.239-67A>G
ENST00000679909.1:c.28+16963A>G	ENSP00000506089.1:n.28+16963A>G
ENST00000453660.3:n.216-67A>G
ENST00000538324.2:c.204-67A>G	ENSP00000483018.1:n.204-67A>G
ENST00000611156.4:c.204-67A>G	ENSP00000483265.1:n.204-67A>G
NM_020469.2:c.204-67A>G	NP_065202.2:n.204-67A>G
NM_020469.3:c.204-67A>G	NP_065202.2:n.204-67A>G