Canonical Allele Identifier: CA1129551922
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1831272130

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872572G>C , CM000671.2:g.130872572G>C GRCh38
NC_000009.11:g.133747959G>C , CM000671.1:g.133747959G>C GRCh37
NC_000009.10:g.132737780G>C NCBI36
NG_012034.1:g.163692G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.965-288G>C ENSP00000361423.2:n.965-288G>C
ENST00000318560.6:c.908-288G>C MANE Select ENSP00000323315.5:n.908-288G>C
ENST00000372348.7:c.965-288G>C ENSP00000361423.2:n.965-288G>C
ENST00000318560.5:c.908-288G>C ENSP00000323315.5:n.908-288G>C
ENST00000372348.6:c.965-288G>C ENSP00000361423.2:n.965-288G>C
NM_005157.5:c.908-288G>C NP_005148.2:n.908-288G>C
NM_007313.2:c.965-288G>C NP_009297.2:n.965-288G>C
NM_005157.6:c.908-288G>C MANE Select NP_005148.2:n.908-288G>C
NM_007313.3:c.965-288G>C NP_009297.2:n.965-288G>C