Canonical Allele Identifier: CA5305864
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs782334638
ExAC: 9:136131765 G / A
gnomAD v2: 9-136131765-G-A
gnomAD v3: 9-133256378-G-A
gnomAD v4: 9-133256378-G-A
MyVariant Identifiers: chr9:g.136131765G>A (hg19) chr9:g.133256378G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256378G>A , CM000671.2:g.133256378G>A GRCh38
NC_000009.11:g.136131765G>A , CM000671.1:g.136131765G>A GRCh37
NC_000009.10:g.135121586G>A NCBI36
NG_006669.1:g.21290C>T
NG_006669.2:g.23838C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.404-22C>T
ENST00000647353.1:n.54-5226C>T
ENST00000651471.1:n.330-22C>T
ENST00000679909.1:c.28+18784C>T ENSP00000506089.1:n.28+18784C>T
ENST00000453660.3:n.386-22C>T
ENST00000538324.2:c.372-22C>T ENSP00000483018.1:n.372-22C>T
ENST00000611156.4:c.372-22C>T ENSP00000483265.1:n.372-22C>T
NM_020469.2:c.375-22C>T NP_065202.2:n.375-22C>T
NM_020469.3:c.375-22C>T NP_065202.2:n.375-22C>T
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