Canonical Allele Identifier: CA375688026

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136137500A>C (hg19) ; chr9:g.133262097A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133262097A>C , CM000671.2:g.133262097A>C	GRCh38
NC_000009.11:g.136137500A>C , CM000671.1:g.136137500A>C	GRCh37
NC_000009.10:g.135127321A>C	NCBI36
NG_006669.1:g.15552T>G
NG_006669.2:g.18118T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.128+2T>G
ENST00000647353.1:n.54-10945T>G
ENST00000651471.1:n.133+2T>G
ENST00000679909.1:c.28+13065T>G	ENSP00000506089.1:n.28+13065T>G
ENST00000453660.3:n.110+2T>G
ENST00000538324.2:c.98+2T>G	ENSP00000483018.1:n.98+2T>G
ENST00000611156.4:c.98+2T>G	ENSP00000483265.1:n.98+2T>G
NM_020469.2:c.98+2T>G	NP_065202.2:n.98+2T>G
NM_020469.3:c.98+2T>G	NP_065202.2:n.98+2T>G