Canonical Allele Identifier: CA467782956
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136131677G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256290G>T , CM000671.2:g.133256290G>T GRCh38
NC_000009.11:g.136131677G>T , CM000671.1:g.136131677G>T GRCh37
NC_000009.10:g.135121498G>T NCBI36
NG_006669.1:g.21378C>A
NG_006669.2:g.23926C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.470C>A
ENST00000647353.1:n.54-5138C>A
ENST00000651471.1:n.396C>A
ENST00000679909.1:c.28+18872C>A ENSP00000506089.1:n.28+18872C>A
ENST00000453660.3:n.452C>A
ENST00000538324.2:c.438C>A ENSP00000483018.1:p.Val146=
ENST00000611156.4:c.438C>A ENSP00000483265.1:p.Val146=
NM_020469.2:c.441C>A NP_065202.2:p.Val147=
NM_020469.3:c.441C>A NP_065202.2:p.Val147=