Canonical Allele Identifier: CA2544283677
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258330A>G , CM000671.2:g.133258330A>G GRCh38
NC_000009.11:g.136133721A>G , CM000671.1:g.136133721A>G GRCh37
NC_000009.10:g.135123542A>G NCBI36
NG_006669.1:g.19333T>C
NG_006669.2:g.21885T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-198T>C
ENST00000647353.1:n.54-7178T>C
ENST00000651471.1:n.239-198T>C
ENST00000679909.1:c.28+16832T>C ENSP00000506089.1:n.28+16832T>C
ENST00000453660.3:n.216-198T>C
ENST00000538324.2:c.204-198T>C ENSP00000483018.1:n.204-198T>C
ENST00000611156.4:c.204-198T>C ENSP00000483265.1:n.204-198T>C
NM_020469.2:c.204-198T>C NP_065202.2:n.204-198T>C
NM_020469.3:c.204-198T>C NP_065202.2:n.204-198T>C