Canonical Allele Identifier: CA1882580560
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256174A= , CM000671.2:g.133256174A= GRCh38
NC_000009.11:g.136131561A= , CM000671.1:g.136131561A= GRCh37
NC_000009.10:g.135121382A= NCBI36
NG_006669.1:g.21494T=
NG_006669.2:g.24042T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.586T=
ENST00000647353.1:n.54-5022T=
ENST00000651471.1:n.512T=
ENST00000679909.1:c.28+18988T= ENSP00000506089.1:n.28+18988T=
ENST00000453660.3:n.568T=
ENST00000538324.2:c.554T= ENSP00000483018.1:p.Met185=
ENST00000611156.4:c.554T= ENSP00000483265.1:p.Met185=
NM_020469.2:c.557T= NP_065202.2:p.Met186=
NM_020469.3:c.557T= NP_065202.2:p.Met186=