Canonical Allele Identifier: CA375686301

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131652G>A (hg19) ; chr9:g.133256265G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256265G>A , CM000671.2:g.133256265G>A	GRCh38
NC_000009.11:g.136131652G>A , CM000671.1:g.136131652G>A	GRCh37
NC_000009.10:g.135121473G>A	NCBI36
NG_006669.1:g.21403C>T
NG_006669.2:g.23951C>T

Transcript Alleles

HGVS	Amino-acid change
NM_020469.2:c.466C>T	NP_065202.2:p.Pro156Ser
NM_020469.3:c.466C>T	NP_065202.2:p.Pro156Ser
ENST00000453660.3:n.477C>T
ENST00000538324.2:c.463C>T	ENSP00000483018.1:p.Pro155Ser
ENST00000611156.4:c.463C>T	ENSP00000483265.1:p.Pro155Ser