Canonical Allele Identifier: CA2692330937

Gene: ABO

Linked Data

• gnomAD v4: 9-133258277-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258277T>C , CM000671.2:g.133258277T>C	GRCh38
NC_000009.11:g.136133668T>C , CM000671.1:g.136133668T>C	GRCh37
NC_000009.10:g.135123489T>C	NCBI36
NG_006669.1:g.19386A>G
NG_006669.2:g.21938A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-145A>G
ENST00000647353.1:n.54-7125A>G
ENST00000651471.1:n.239-145A>G
ENST00000679909.1:c.28+16885A>G	ENSP00000506089.1:n.28+16885A>G
ENST00000453660.3:n.216-145A>G
ENST00000538324.2:c.204-145A>G	ENSP00000483018.1:n.204-145A>G
ENST00000611156.4:c.204-145A>G	ENSP00000483265.1:n.204-145A>G
NM_020469.2:c.204-145A>G	NP_065202.2:n.204-145A>G
NM_020469.3:c.204-145A>G	NP_065202.2:n.204-145A>G