Canonical Allele Identifier: CA467853029

Gene: ABO

Linked Data

• MyVariant Identifiers: chr9:g.136131499G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133256112G>A , CM000671.2:g.133256112G>A	GRCh38
NC_000009.11:g.136131499G>A , CM000671.1:g.136131499G>A	GRCh37
NC_000009.10:g.135121320G>A	NCBI36
NG_006669.1:g.21556C>T
NG_006669.2:g.24104C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453660.4:n.648C>T
ENST00000647353.1:n.54-4960C>T
ENST00000651471.1:n.574C>T
ENST00000679909.1:c.28+19050C>T	ENSP00000506089.1:n.28+19050C>T
ENST00000453660.3:n.630C>T
ENST00000538324.2:c.616C>T	ENSP00000483018.1:p.Leu206=
ENST00000611156.4:c.616C>T	ENSP00000483265.1:p.Leu206=
NM_020469.2:c.619C>T	NP_065202.2:p.Leu207=
NM_020469.3:c.619C>T	NP_065202.2:p.Leu207=