Canonical Allele Identifier: CA467780435
Gene: ABO HGNC NCBI

Linked Data

gnomAD v4: 9-133255395-T-G
MyVariant Identifiers: chr9:g.136130782T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255395T>G , CM000671.2:g.133255395T>G GRCh38
NC_000009.11:g.136130782T>G , CM000671.1:g.136130782T>G GRCh37
NC_000009.10:g.135120603T>G NCBI36
NG_006669.1:g.22273A>C
NG_006669.2:g.24821A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1365A>C
ENST00000647353.1:n.54-4243A>C
ENST00000679909.1:c.28+19767A>C ENSP00000506089.1:n.28+19767A>C
ENST00000453660.3:n.1347A>C
ENST00000611156.4:c.*271A>C ENSP00000483265.1:n.*271A>C
NM_020469.2:c.*271A>C NP_065202.2:n.*271A>C
NM_020469.3:c.*271A>C NP_065202.2:n.*271A>C
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