Canonical Allele Identifier: CA467780683
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1195265125
gnomAD v3: 9-133255429-G-A
gnomAD v4: 9-133255429-G-A
MyVariant Identifiers: chr9:g.136130816G>A (hg19) chr9:g.133255429G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133255429G>A , CM000671.2:g.133255429G>A GRCh38
NC_000009.11:g.136130816G>A , CM000671.1:g.136130816G>A GRCh37
NC_000009.10:g.135120637G>A NCBI36
NG_006669.1:g.22239C>T
NG_006669.2:g.24787C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.1331C>T
ENST00000647353.1:n.54-4277C>T
ENST00000679909.1:c.28+19733C>T ENSP00000506089.1:n.28+19733C>T
ENST00000453660.3:n.1313C>T
ENST00000611156.4:c.*237C>T ENSP00000483265.1:n.*237C>T
NM_020469.2:c.*237C>T NP_065202.2:n.*237C>T
NM_020469.3:c.*237C>T NP_065202.2:n.*237C>T
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