Canonical Allele Identifier: CA2579497386

Gene: ABO

Linked Data

• gnomAD v4: 9-133258000-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258000G>T , CM000671.2:g.133258000G>T	GRCh38
NC_000009.11:g.136133390G>T , CM000671.1:g.136133390G>T	GRCh37
NC_000009.10:g.135123211G>T	NCBI36
NG_006669.1:g.19664C>A
NG_006669.2:g.22215C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.269+97C>A
ENST00000647353.1:n.54-6848C>A
ENST00000651471.1:n.329+42C>A
ENST00000679909.1:c.28+17162C>A	ENSP00000506089.1:n.28+17162C>A
ENST00000453660.3:n.251+97C>A
ENST00000538324.2:c.239+97C>A	ENSP00000483018.1:n.239+97C>A
ENST00000611156.4:c.239+97C>A	ENSP00000483265.1:n.239+97C>A
NM_020469.2:c.239+97C>A	NP_065202.2:n.239+97C>A
NM_020469.3:c.239+97C>A	NP_065202.2:n.239+97C>A