Canonical Allele Identifier: CA375686007

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131513C>A (hg19) ; chr9:g.133256126C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256126C>A , CM000671.2:g.133256126C>A	GRCh38
NC_000009.11:g.136131513C>A , CM000671.1:g.136131513C>A	GRCh37
NC_000009.10:g.135121334C>A	NCBI36
NG_006669.1:g.21542G>T
NG_006669.2:g.24090G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.634G>T
ENST00000647353.1:n.54-4974G>T
ENST00000651471.1:n.560G>T
ENST00000679909.1:c.28+19036G>T	ENSP00000506089.1:n.28+19036G>T
ENST00000453660.3:n.616G>T
ENST00000538324.2:c.602G>T	ENSP00000483018.1:p.Ser201Ile
ENST00000611156.4:c.602G>T	ENSP00000483265.1:p.Ser201Ile
NM_020469.2:c.605G>T	NP_065202.2:p.Ser202Ile
NM_020469.3:c.605G>T	NP_065202.2:p.Ser202Ile