Canonical Allele Identifier: CA375686323

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131662G>T (hg19) ; chr9:g.133256275G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256275G>T , CM000671.2:g.133256275G>T	GRCh38
NC_000009.11:g.136131662G>T , CM000671.1:g.136131662G>T	GRCh37
NC_000009.10:g.135121483G>T	NCBI36
NG_006669.1:g.21393C>A
NG_006669.2:g.23941C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453660.4:n.485C>A
ENST00000647353.1:n.54-5123C>A
ENST00000651471.1:n.411C>A
ENST00000679909.1:c.28+18887C>A	ENSP00000506089.1:n.28+18887C>A
ENST00000453660.3:n.467C>A
ENST00000538324.2:c.453C>A	ENSP00000483018.1:p.Phe151Leu
ENST00000611156.4:c.453C>A	ENSP00000483265.1:p.Phe151Leu
NM_020469.2:c.456C>A	NP_065202.2:p.Phe152Leu
NM_020469.3:c.456C>A	NP_065202.2:p.Phe152Leu