Canonical Allele Identifier: CA860755325

Gene: ABO

Linked Data

• dbSNP Id: rs1204599093
• gnomAD v4: 9-133258240-C-G
• MyVariant Identifiers: chr9:g.136133631C>G (hg19) ; chr9:g.133258240C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258240C>G , CM000671.2:g.133258240C>G	GRCh38
NC_000009.11:g.136133631C>G , CM000671.1:g.136133631C>G	GRCh37
NC_000009.10:g.135123452C>G	NCBI36
NG_006669.1:g.19423G>C
NG_006669.2:g.21975G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-108G>C
ENST00000647353.1:n.54-7088G>C
ENST00000651471.1:n.239-108G>C
ENST00000679909.1:c.28+16922G>C	ENSP00000506089.1:n.28+16922G>C
ENST00000453660.3:n.216-108G>C
ENST00000538324.2:c.204-108G>C	ENSP00000483018.1:n.204-108G>C
ENST00000611156.4:c.204-108G>C	ENSP00000483265.1:n.204-108G>C
NM_020469.2:c.204-108G>C	NP_065202.2:n.204-108G>C
NM_020469.3:c.204-108G>C	NP_065202.2:n.204-108G>C