Canonical Allele Identifier: CA375686845

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136133500C>T (hg19) ; chr9:g.133258110C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133258110C>T , CM000671.2:g.133258110C>T	GRCh38
NC_000009.11:g.136133500C>T , CM000671.1:g.136133500C>T	GRCh37
NC_000009.10:g.135123321C>T	NCBI36
NG_006669.1:g.19554G>A
NG_006669.2:g.22105G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.256G>A
ENST00000647353.1:n.54-6958G>A
ENST00000651471.1:n.261G>A
ENST00000679909.1:c.28+17052G>A	ENSP00000506089.1:n.28+17052G>A
ENST00000453660.3:n.238G>A
ENST00000538324.2:c.226G>A	ENSP00000483018.1:p.Val76Met
ENST00000611156.4:c.226G>A	ENSP00000483265.1:p.Val76Met
NM_020469.2:c.226G>A	NP_065202.2:p.Val76Met
NM_020469.3:c.226G>A	NP_065202.2:p.Val76Met