Canonical Allele Identifier: CA467780137
Gene: ABO HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.136130735C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255348C>T , CM000671.2:g.133255348C>T GRCh38
NC_000009.11:g.136130735C>T , CM000671.1:g.136130735C>T GRCh37
NC_000009.10:g.135120556C>T NCBI36
NG_006669.1:g.22320G>A
NG_006669.2:g.24868G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1412G>A
ENST00000647353.1:n.54-4196G>A
ENST00000679909.1:c.28+19814G>A ENSP00000506089.1:n.28+19814G>A
ENST00000453660.3:n.1394G>A
ENST00000611156.4:c.*318G>A ENSP00000483265.1:n.*318G>A
NM_020469.2:c.*318G>A NP_065202.2:n.*318G>A
NM_020469.3:c.*318G>A NP_065202.2:n.*318G>A
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