Canonical Allele Identifier: CA375686743

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136132899G>T (hg19) ; chr9:g.133257512G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133257512G>T , CM000671.2:g.133257512G>T	GRCh38
NC_000009.11:g.136132899G>T , CM000671.1:g.136132899G>T	GRCh37
NC_000009.10:g.135122720G>T	NCBI36
NG_006669.1:g.20156C>A
NG_006669.2:g.22704C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.300C>A
ENST00000647353.1:n.54-6360C>A
ENST00000651471.1:n.329+530C>A
ENST00000679909.1:c.28+17650C>A	ENSP00000506089.1:n.28+17650C>A
ENST00000453660.3:n.282C>A
ENST00000538324.2:c.268C>A	ENSP00000483018.1:p.Leu90Met
ENST00000611156.4:c.268C>A	ENSP00000483265.1:p.Leu90Met
NM_020469.2:c.271C>A	NP_065202.2:p.Leu91Met
NM_020469.3:c.271C>A	NP_065202.2:p.Leu91Met