Canonical Allele Identifier: CA5305855
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs566935663
ExAC: 9:136131755 G / A
gnomAD v2: 9-136131755-G-A
gnomAD v3: 9-133256368-G-A
gnomAD v4: 9-133256368-G-A
MyVariant Identifiers: chr9:g.136131755G>A (hg19) chr9:g.133256368G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256368G>A , CM000671.2:g.133256368G>A GRCh38
NC_000009.11:g.136131755G>A , CM000671.1:g.136131755G>A GRCh37
NC_000009.10:g.135121576G>A NCBI36
NG_006669.1:g.21300C>T
NG_006669.2:g.23848C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.404-12C>T
ENST00000647353.1:n.54-5216C>T
ENST00000651471.1:n.330-12C>T
ENST00000679909.1:c.28+18794C>T ENSP00000506089.1:n.28+18794C>T
ENST00000453660.3:n.386-12C>T
ENST00000538324.2:c.372-12C>T ENSP00000483018.1:n.372-12C>T
ENST00000611156.4:c.372-12C>T ENSP00000483265.1:n.372-12C>T
NM_020469.2:c.375-12C>T NP_065202.2:n.375-12C>T
NM_020469.3:c.375-12C>T NP_065202.2:n.375-12C>T
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