Canonical Allele Identifier: CA2692330379

Gene: ABO

Linked Data

• gnomAD v4: 9-133256400-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256400C>A , CM000671.2:g.133256400C>A	GRCh38
NC_000009.11:g.136131787C>A , CM000671.1:g.136131787C>A	GRCh37
NC_000009.10:g.135121608C>A	NCBI36
NG_006669.1:g.21268G>T
NG_006669.2:g.23816G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.404-44G>T
ENST00000647353.1:n.54-5248G>T
ENST00000651471.1:n.330-44G>T
ENST00000679909.1:c.28+18762G>T	ENSP00000506089.1:n.28+18762G>T
ENST00000453660.3:n.386-44G>T
ENST00000538324.2:c.372-44G>T	ENSP00000483018.1:n.372-44G>T
ENST00000611156.4:c.372-44G>T	ENSP00000483265.1:n.372-44G>T
NM_020469.2:c.375-44G>T	NP_065202.2:n.375-44G>T
NM_020469.3:c.375-44G>T	NP_065202.2:n.375-44G>T