Canonical Allele Identifier: CA5305873
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs367841195
ExAC: 9:136131780 G / C
gnomAD v2: 9-136131780-G-C
gnomAD v3: 9-133256393-G-C
gnomAD v4: 9-133256393-G-C
MyVariant Identifiers: chr9:g.136131780G>C (hg19) chr9:g.133256393G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133256393G>C , CM000671.2:g.133256393G>C GRCh38
NC_000009.11:g.136131780G>C , CM000671.1:g.136131780G>C GRCh37
NC_000009.10:g.135121601G>C NCBI36
NG_006669.1:g.21275C>G
NG_006669.2:g.23823C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.404-37C>G
ENST00000647353.1:n.54-5241C>G
ENST00000651471.1:n.330-37C>G
ENST00000679909.1:c.28+18769C>G ENSP00000506089.1:n.28+18769C>G
ENST00000453660.3:n.386-37C>G
ENST00000538324.2:c.372-37C>G ENSP00000483018.1:n.372-37C>G
ENST00000611156.4:c.372-37C>G ENSP00000483265.1:n.372-37C>G
NM_020469.2:c.375-37C>G NP_065202.2:n.375-37C>G
NM_020469.3:c.375-37C>G NP_065202.2:n.375-37C>G
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