Canonical Allele Identifier: CA467782880

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131599C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256212C>A , CM000671.2:g.133256212C>A	GRCh38
NC_000009.11:g.136131599C>A , CM000671.1:g.136131599C>A	GRCh37
NC_000009.10:g.135121420C>A	NCBI36
NG_006669.1:g.21456G>T
NG_006669.2:g.24004G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.548G>T
ENST00000647353.1:n.54-5060G>T
ENST00000651471.1:n.474G>T
ENST00000679909.1:c.28+18950G>T	ENSP00000506089.1:n.28+18950G>T
ENST00000453660.3:n.530G>T
ENST00000538324.2:c.516G>T	ENSP00000483018.1:p.Leu172=
ENST00000611156.4:c.516G>T	ENSP00000483265.1:p.Leu172=
NM_020469.2:c.519G>T	NP_065202.2:p.Leu173=
NM_020469.3:c.519G>T	NP_065202.2:p.Leu173=