Canonical Allele Identifier: CA467395024

Gene: ABL1

Linked Data

• MyVariant Identifiers: chr9:g.133748248G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872861G>C , CM000671.2:g.130872861G>C	GRCh38
NC_000009.11:g.133748248G>C , CM000671.1:g.133748248G>C	GRCh37
NC_000009.10:g.132738069G>C	NCBI36
NG_012034.1:g.163981G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372348.9:c.966G>C	ENSP00000361423.2:p.Gly322=
ENST00000318560.6:c.909G>C MANE Select	ENSP00000323315.5:p.Gly303=
ENST00000372348.7:c.966G>C	ENSP00000361423.2:p.Gly322=
ENST00000318560.5:c.909G>C	ENSP00000323315.5:p.Gly303=
ENST00000372348.6:c.966G>C	ENSP00000361423.2:p.Gly322=
NM_005157.5:c.909G>C	NP_005148.2:p.Gly303=
NM_007313.2:c.966G>C	NP_009297.2:p.Gly322=
NM_005157.6:c.909G>C MANE Select	NP_005148.2:p.Gly303=
NM_007313.3:c.966G>C	NP_009297.2:p.Gly322=