Canonical Allele Identifier: CA467496376

Gene: ABL1

Linked Data

• ClinVar Variation Id: 2962526
• ClinVar RCV Id: RCV003825156
• dbSNP Id: rs1831100097
• gnomAD v4: 9-130862975-G-A
• MyVariant Identifiers: chr9:g.133738362G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130862975G>A , CM000671.2:g.130862975G>A	GRCh38
NC_000009.11:g.133738362G>A , CM000671.1:g.133738362G>A	GRCh37
NC_000009.10:g.132728183G>A	NCBI36
NG_012034.1:g.154095G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.819G>A	ENSP00000361423.2:p.Gly273=
ENST00000318560.6:c.762G>A MANE Select	ENSP00000323315.5:p.Gly254=
ENST00000372348.7:c.819G>A	ENSP00000361423.2:p.Gly273=
ENST00000318560.5:c.762G>A	ENSP00000323315.5:p.Gly254=
ENST00000372348.6:c.819G>A	ENSP00000361423.2:p.Gly273=
NM_005157.5:c.762G>A	NP_005148.2:p.Gly254=
NM_007313.2:c.819G>A	NP_009297.2:p.Gly273=
NM_005157.6:c.762G>A MANE Select	NP_005148.2:p.Gly254=
NM_007313.3:c.819G>A	NP_009297.2:p.Gly273=