Canonical Allele Identifier: CA200766518
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs575088257
gnomAD v2: 9-136133801-G-A
gnomAD v3: 9-133258410-G-A
gnomAD v4: 9-133258410-G-A
MyVariant Identifiers: chr9:g.136133801G>A (hg19) chr9:g.133258410G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133258410G>A , CM000671.2:g.133258410G>A GRCh38
NC_000009.11:g.136133801G>A , CM000671.1:g.136133801G>A GRCh37
NC_000009.10:g.135123622G>A NCBI36
NG_006669.1:g.19253C>T
NG_006669.2:g.21805C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000453660.4:n.234-278C>T
ENST00000647353.1:n.54-7258C>T
ENST00000651471.1:n.239-278C>T
ENST00000679909.1:c.28+16752C>T ENSP00000506089.1:n.28+16752C>T
ENST00000453660.3:n.216-278C>T
ENST00000538324.2:c.204-278C>T ENSP00000483018.1:n.204-278C>T
ENST00000611156.4:c.204-278C>T ENSP00000483265.1:n.204-278C>T
NM_020469.2:c.204-278C>T NP_065202.2:n.204-278C>T
NM_020469.3:c.204-278C>T NP_065202.2:n.204-278C>T
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