Canonical Allele Identifier: CA2720457332
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs544850559

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872821C>A , CM000671.2:g.130872821C>A GRCh38
NC_000009.11:g.133748208C>A , CM000671.1:g.133748208C>A GRCh37
NC_000009.10:g.132738029C>A NCBI36
NG_012034.1:g.163941C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.965-39C>A ENSP00000361423.2:n.965-39C>A
ENST00000318560.6:c.908-39C>A MANE Select ENSP00000323315.5:n.908-39C>A
ENST00000372348.7:c.965-39C>A ENSP00000361423.2:n.965-39C>A
ENST00000318560.5:c.908-39C>A ENSP00000323315.5:n.908-39C>A
ENST00000372348.6:c.965-39C>A ENSP00000361423.2:n.965-39C>A
NM_005157.5:c.908-39C>A NP_005148.2:n.908-39C>A
NM_007313.2:c.965-39C>A NP_009297.2:n.965-39C>A
NM_005157.6:c.908-39C>A MANE Select NP_005148.2:n.908-39C>A
NM_007313.3:c.965-39C>A NP_009297.2:n.965-39C>A