Canonical Allele Identifier: CA2692330774

Gene: ABO

Linked Data

• gnomAD v4: 9-133258010-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258010A>C , CM000671.2:g.133258010A>C	GRCh38
NC_000009.11:g.136133400A>C , CM000671.1:g.136133400A>C	GRCh37
NC_000009.10:g.135123221A>C	NCBI36
NG_006669.1:g.19654T>G
NG_006669.2:g.22205T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.269+87T>G
ENST00000647353.1:n.54-6858T>G
ENST00000651471.1:n.329+32T>G
ENST00000679909.1:c.28+17152T>G	ENSP00000506089.1:n.28+17152T>G
ENST00000453660.3:n.251+87T>G
ENST00000538324.2:c.239+87T>G	ENSP00000483018.1:n.239+87T>G
ENST00000611156.4:c.239+87T>G	ENSP00000483265.1:n.239+87T>G
NM_020469.2:c.239+87T>G	NP_065202.2:n.239+87T>G
NM_020469.3:c.239+87T>G	NP_065202.2:n.239+87T>G