Canonical Allele Identifier: CA467784338
Gene: ABO HGNC NCBI

Linked Data

dbSNP Id: rs1834680588
MyVariant Identifiers: chr9:g.136135483G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133260079G>A , CM000671.2:g.133260079G>A GRCh38
NC_000009.11:g.136135483G>A , CM000671.1:g.136135483G>A GRCh37
NC_000009.10:g.135125304G>A NCBI36
NG_006669.1:g.17571C>T
NG_006669.2:g.20136C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000453660.4:n.186-213C>T
ENST00000647353.1:n.54-8927C>T
ENST00000651471.1:n.191-213C>T
ENST00000679909.1:c.28+15083C>T ENSP00000506089.1:n.28+15083C>T
ENST00000453660.3:n.168-213C>T
ENST00000538324.2:c.156-213C>T ENSP00000483018.1:n.156-213C>T
ENST00000611156.4:c.156-213C>T ENSP00000483265.1:n.156-213C>T
NM_020469.2:c.156-213C>T NP_065202.2:n.156-213C>T
NM_020469.3:c.156-213C>T NP_065202.2:n.156-213C>T
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