Canonical Allele Identifier: CA860511721

Gene: ABL1

Linked Data

• dbSNP Id: rs1260852282
• MyVariant Identifiers: chr9:g.133748130T>C (hg19) ; chr9:g.130872743T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872743T>C , CM000671.2:g.130872743T>C	GRCh38
NC_000009.11:g.133748130T>C , CM000671.1:g.133748130T>C	GRCh37
NC_000009.10:g.132737951T>C	NCBI36
NG_012034.1:g.163863T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.965-117T>C	ENSP00000361423.2:n.965-117T>C
ENST00000318560.6:c.908-117T>C MANE Select	ENSP00000323315.5:n.908-117T>C
ENST00000372348.7:c.965-117T>C	ENSP00000361423.2:n.965-117T>C
ENST00000318560.5:c.908-117T>C	ENSP00000323315.5:n.908-117T>C
ENST00000372348.6:c.965-117T>C	ENSP00000361423.2:n.965-117T>C
NM_005157.5:c.908-117T>C	NP_005148.2:n.908-117T>C
NM_007313.2:c.965-117T>C	NP_009297.2:n.965-117T>C
NM_005157.6:c.908-117T>C MANE Select	NP_005148.2:n.908-117T>C
NM_007313.3:c.965-117T>C	NP_009297.2:n.965-117T>C