Canonical Allele Identifier: CA467853013
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136131482C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256095C>A , CM000671.2:g.133256095C>A GRCh38
NC_000009.11:g.136131482C>A , CM000671.1:g.136131482C>A GRCh37
NC_000009.10:g.135121303C>A NCBI36
NG_006669.1:g.21573G>T
NG_006669.2:g.24121G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.665G>T
ENST00000647353.1:n.54-4943G>T
ENST00000679909.1:c.28+19067G>T ENSP00000506089.1:n.28+19067G>T
ENST00000453660.3:n.647G>T
ENST00000538324.2:c.633G>T ENSP00000483018.1:p.Val211=
ENST00000611156.4:c.633G>T ENSP00000483265.1:p.Val211=
NM_020469.2:c.636G>T NP_065202.2:p.Val212=
NM_020469.3:c.636G>T NP_065202.2:p.Val212=