Canonical Allele Identifier: CA860511695

Gene: ABL1

Linked Data

• dbSNP Id: rs1400155409
• MyVariant Identifiers: chr9:g.133748064G>T (hg19) ; chr9:g.130872677G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.130872677G>T , CM000671.2:g.130872677G>T	GRCh38
NC_000009.11:g.133748064G>T , CM000671.1:g.133748064G>T	GRCh37
NC_000009.10:g.132737885G>T	NCBI36
NG_012034.1:g.163797G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372348.9:c.965-183G>T	ENSP00000361423.2:n.965-183G>T
ENST00000318560.6:c.908-183G>T MANE Select	ENSP00000323315.5:n.908-183G>T
ENST00000372348.7:c.965-183G>T	ENSP00000361423.2:n.965-183G>T
ENST00000318560.5:c.908-183G>T	ENSP00000323315.5:n.908-183G>T
ENST00000372348.6:c.965-183G>T	ENSP00000361423.2:n.965-183G>T
NM_005157.5:c.908-183G>T	NP_005148.2:n.908-183G>T
NM_007313.2:c.965-183G>T	NP_009297.2:n.965-183G>T
NM_005157.6:c.908-183G>T MANE Select	NP_005148.2:n.908-183G>T
NM_007313.3:c.965-183G>T	NP_009297.2:n.965-183G>T