Canonical Allele Identifier: CA375685798
Gene: ABO HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256089C>G , CM000671.2:g.133256089C>G GRCh38
NC_000009.11:g.136131476C>G , CM000671.1:g.136131476C>G GRCh37
NC_000009.10:g.135121297C>G NCBI36
NG_006669.1:g.21579G>C
NG_006669.2:g.24127G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.671G>C
ENST00000647353.1:n.54-4937G>C
ENST00000679909.1:c.28+19073G>C ENSP00000506089.1:n.28+19073G>C
ENST00000453660.3:n.653G>C
ENST00000538324.2:c.639G>C ENSP00000483018.1:p.Met213Ile
ENST00000611156.4:c.639G>C ENSP00000483265.1:p.Met213Ile
NM_020469.2:c.642G>C NP_065202.2:p.Met214Ile
NM_020469.3:c.642G>C NP_065202.2:p.Met214Ile