Canonical Allele Identifier: CA375262508
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs2132973552

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862835G>A , CM000671.2:g.130862835G>A GRCh38
NC_000009.11:g.133738222G>A , CM000671.1:g.133738222G>A GRCh37
NC_000009.10:g.132728043G>A NCBI36
NG_012034.1:g.153955G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.679G>A ENSP00000361423.2:p.Gly227Arg
ENST00000318560.6:c.622G>A MANE Select ENSP00000323315.5:p.Gly208Arg
ENST00000372348.7:c.679G>A ENSP00000361423.2:p.Gly227Arg
ENST00000318560.5:c.622G>A ENSP00000323315.5:p.Gly208Arg
ENST00000372348.6:c.679G>A ENSP00000361423.2:p.Gly227Arg
NM_005157.5:c.622G>A NP_005148.2:p.Gly208Arg
NM_007313.2:c.679G>A NP_009297.2:p.Gly227Arg
NM_005157.6:c.622G>A MANE Select NP_005148.2:p.Gly208Arg
NM_007313.3:c.679G>A NP_009297.2:p.Gly227Arg