Canonical Allele Identifier: CA860755335

Gene: ABO

Linked Data

• dbSNP Id: rs1203686670
• gnomAD v4: 9-133258243-G-C
• MyVariant Identifiers: chr9:g.136133634G>C (hg19) ; chr9:g.133258243G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258243G>C , CM000671.2:g.133258243G>C	GRCh38
NC_000009.11:g.136133634G>C , CM000671.1:g.136133634G>C	GRCh37
NC_000009.10:g.135123455G>C	NCBI36
NG_006669.1:g.19420C>G
NG_006669.2:g.21972C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.234-111C>G
ENST00000647353.1:n.54-7091C>G
ENST00000651471.1:n.239-111C>G
ENST00000679909.1:c.28+16919C>G	ENSP00000506089.1:n.28+16919C>G
ENST00000453660.3:n.216-111C>G
ENST00000538324.2:c.204-111C>G	ENSP00000483018.1:n.204-111C>G
ENST00000611156.4:c.204-111C>G	ENSP00000483265.1:n.204-111C>G
NM_020469.2:c.204-111C>G	NP_065202.2:n.204-111C>G
NM_020469.3:c.204-111C>G	NP_065202.2:n.204-111C>G