Canonical Allele Identifier: CA200767664

Gene: ABO

Linked Data

• dbSNP Id: rs911773249
• gnomAD v2: 9-136137087-C-T
• gnomAD v3: 9-133261684-C-T
• gnomAD v4: 9-133261684-C-T
• MyVariant Identifiers: chr9:g.136137087C>T (hg19) ; chr9:g.133261684C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133261684C>T , CM000671.2:g.133261684C>T	GRCh38
NC_000009.11:g.136137087C>T , CM000671.1:g.136137087C>T	GRCh37
NC_000009.10:g.135126908C>T	NCBI36
NG_006669.1:g.15966G>A
NG_006669.2:g.18531G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.129-310G>A
ENST00000647353.1:n.54-10532G>A
ENST00000651471.1:n.134-310G>A
ENST00000679909.1:c.28+13478G>A	ENSP00000506089.1:n.28+13478G>A
ENST00000453660.3:n.111-310G>A
ENST00000538324.2:c.99-310G>A	ENSP00000483018.1:n.99-310G>A
ENST00000611156.4:c.99-310G>A	ENSP00000483265.1:n.99-310G>A
NM_020469.2:c.99-310G>A	NP_065202.2:n.99-310G>A
NM_020469.3:c.99-310G>A	NP_065202.2:n.99-310G>A