Canonical Allele Identifier: CA467780053
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130709G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255322G>T , CM000671.2:g.133255322G>T GRCh38
NC_000009.11:g.136130709G>T , CM000671.1:g.136130709G>T GRCh37
NC_000009.10:g.135120530G>T NCBI36
NG_006669.1:g.22346C>A
NG_006669.2:g.24894C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1438C>A
ENST00000647353.1:n.54-4170C>A
ENST00000679909.1:c.28+19840C>A ENSP00000506089.1:n.28+19840C>A
ENST00000453660.3:n.1420C>A
ENST00000611156.4:c.*344C>A ENSP00000483265.1:n.*344C>A
NM_020469.2:c.*344C>A NP_065202.2:n.*344C>A
NM_020469.3:c.*344C>A NP_065202.2:n.*344C>A
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