Canonical Allele Identifier: CA200766362
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs979670939
gnomAD v2: 9-136133420-G-A
gnomAD v3: 9-133258030-G-A
gnomAD v4: 9-133258030-G-A
MyVariant Identifiers: chr9:g.136133420G>A (hg19) chr9:g.133258030G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258030G>A , CM000671.2:g.133258030G>A GRCh38
NC_000009.11:g.136133420G>A , CM000671.1:g.136133420G>A GRCh37
NC_000009.10:g.135123241G>A NCBI36
NG_006669.1:g.19634C>T
NG_006669.2:g.22185C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.269+67C>T
ENST00000647353.1:n.54-6878C>T
ENST00000651471.1:n.329+12C>T
ENST00000679909.1:c.28+17132C>T ENSP00000506089.1:n.28+17132C>T
ENST00000453660.3:n.251+67C>T
ENST00000538324.2:c.239+67C>T ENSP00000483018.1:n.239+67C>T
ENST00000611156.4:c.239+67C>T ENSP00000483265.1:n.239+67C>T
NM_020469.2:c.239+67C>T NP_065202.2:n.239+67C>T
NM_020469.3:c.239+67C>T NP_065202.2:n.239+67C>T
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