Canonical Allele Identifier: CA467496318

Gene: ABL1

Linked Data

• dbSNP Id: rs1831098360
• MyVariant Identifiers: chr9:g.133738314A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862927A>G , CM000671.2:g.130862927A>G	GRCh38
NC_000009.11:g.133738314A>G , CM000671.1:g.133738314A>G	GRCh37
NC_000009.10:g.132728135A>G	NCBI36
NG_012034.1:g.154047A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.771A>G	ENSP00000361423.2:p.Glu257=
ENST00000318560.6:c.714A>G MANE Select	ENSP00000323315.5:p.Glu238=
ENST00000372348.7:c.771A>G	ENSP00000361423.2:p.Glu257=
ENST00000318560.5:c.714A>G	ENSP00000323315.5:p.Glu238=
ENST00000372348.6:c.771A>G	ENSP00000361423.2:p.Glu257=
NM_005157.5:c.714A>G	NP_005148.2:p.Glu238=
NM_007313.2:c.771A>G	NP_009297.2:p.Glu257=
NM_005157.6:c.714A>G MANE Select	NP_005148.2:p.Glu238=
NM_007313.3:c.771A>G	NP_009297.2:p.Glu257=