Canonical Allele Identifier: CA2692330366

Gene: ABO

Linked Data

• gnomAD v4: 9-133256359-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256359G>A , CM000671.2:g.133256359G>A	GRCh38
NC_000009.11:g.136131746G>A , CM000671.1:g.136131746G>A	GRCh37
NC_000009.10:g.135121567G>A	NCBI36
NG_006669.1:g.21309C>T
NG_006669.2:g.23857C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.404-3C>T
ENST00000647353.1:n.54-5207C>T
ENST00000651471.1:n.330-3C>T
ENST00000679909.1:c.28+18803C>T	ENSP00000506089.1:n.28+18803C>T
ENST00000453660.3:n.386-3C>T
ENST00000538324.2:c.372-3C>T	ENSP00000483018.1:n.372-3C>T
ENST00000611156.4:c.372-3C>T	ENSP00000483265.1:n.372-3C>T
NM_020469.2:c.375-3C>T	NP_065202.2:n.375-3C>T
NM_020469.3:c.375-3C>T	NP_065202.2:n.375-3C>T