Canonical Allele Identifier: CA375682204
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255616G>C , CM000671.2:g.133255616G>C GRCh38
NC_000009.11:g.136131003G>C , CM000671.1:g.136131003G>C GRCh37
NC_000009.10:g.135120824G>C NCBI36
NG_006669.1:g.22052C>G
NG_006669.2:g.24600C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.1144C>G
ENST00000647353.1:n.54-4464C>G
ENST00000679909.1:c.28+19546C>G ENSP00000506089.1:n.28+19546C>G
ENST00000453660.3:n.1126C>G
ENST00000538324.2:c.1108C>G ENSP00000483018.1:p.Arg370Gly
ENST00000611156.4:c.*50C>G ENSP00000483265.1:n.*50C>G
NM_020469.2:c.*50C>G NP_065202.2:n.*50C>G
NM_020469.3:c.*50C>G NP_065202.2:n.*50C>G