Canonical Allele Identifier: CA860511701

Gene: ABL1

Linked Data

• dbSNP Id: rs1361373780
• gnomAD v3: 9-130872695-C-A
• gnomAD v4: 9-130872695-C-A
• MyVariant Identifiers: chr9:g.133748082C>A (hg19) ; chr9:g.130872695C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872695C>A , CM000671.2:g.130872695C>A	GRCh38
NC_000009.11:g.133748082C>A , CM000671.1:g.133748082C>A	GRCh37
NC_000009.10:g.132737903C>A	NCBI36
NG_012034.1:g.163815C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.965-165C>A	ENSP00000361423.2:n.965-165C>A
ENST00000318560.6:c.908-165C>A MANE Select	ENSP00000323315.5:n.908-165C>A
ENST00000372348.7:c.965-165C>A	ENSP00000361423.2:n.965-165C>A
ENST00000318560.5:c.908-165C>A	ENSP00000323315.5:n.908-165C>A
ENST00000372348.6:c.965-165C>A	ENSP00000361423.2:n.965-165C>A
NM_005157.5:c.908-165C>A	NP_005148.2:n.908-165C>A
NM_007313.2:c.965-165C>A	NP_009297.2:n.965-165C>A
NM_005157.6:c.908-165C>A MANE Select	NP_005148.2:n.908-165C>A
NM_007313.3:c.965-165C>A	NP_009297.2:n.965-165C>A