Canonical Allele Identifier: CA1882580588
Gene: ABO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256181C= , CM000671.2:g.133256181C= GRCh38
NC_000009.11:g.136131568C= , CM000671.1:g.136131568C= GRCh37
NC_000009.10:g.135121389C= NCBI36
NG_006669.1:g.21487G=
NG_006669.2:g.24035G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.579G=
ENST00000647353.1:n.54-5029G=
ENST00000651471.1:n.505G=
ENST00000679909.1:c.28+18981G= ENSP00000506089.1:n.28+18981G=
ENST00000453660.3:n.561G=
ENST00000538324.2:c.547G= ENSP00000483018.1:p.Val183=
ENST00000611156.4:c.547G= ENSP00000483265.1:p.Val183=
NM_020469.2:c.550G= NP_065202.2:p.Val184=
NM_020469.3:c.550G= NP_065202.2:p.Val184=