Canonical Allele Identifier: CA1881474937
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1831267807

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872438G>A , CM000671.2:g.130872438G>A GRCh38
NC_000009.11:g.133747825G>A , CM000671.1:g.133747825G>A GRCh37
NC_000009.10:g.132737646G>A NCBI36
NG_012034.1:g.163558G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+225G>A ENSP00000361423.2:n.964+225G>A
ENST00000318560.6:c.907+225G>A MANE Select ENSP00000323315.5:n.907+225G>A
ENST00000372348.7:c.964+225G>A ENSP00000361423.2:n.964+225G>A
ENST00000318560.5:c.907+225G>A ENSP00000323315.5:n.907+225G>A
ENST00000372348.6:c.964+225G>A ENSP00000361423.2:n.964+225G>A
NM_005157.5:c.907+225G>A NP_005148.2:n.907+225G>A
NM_007313.2:c.964+225G>A NP_009297.2:n.964+225G>A
NM_005157.6:c.907+225G>A MANE Select NP_005148.2:n.907+225G>A
NM_007313.3:c.964+225G>A NP_009297.2:n.964+225G>A