Canonical Allele Identifier: CA467496312
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs2132973890
MyVariant Identifiers: chr9:g.133738308G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130862921G>A , CM000671.2:g.130862921G>A GRCh38
NC_000009.11:g.133738308G>A , CM000671.1:g.133738308G>A GRCh37
NC_000009.10:g.132728129G>A NCBI36
NG_012034.1:g.154041G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.765G>A ENSP00000361423.2:p.Glu255=
ENST00000318560.6:c.708G>A MANE Select ENSP00000323315.5:p.Glu236=
ENST00000372348.7:c.765G>A ENSP00000361423.2:p.Glu255=
ENST00000318560.5:c.708G>A ENSP00000323315.5:p.Glu236=
ENST00000372348.6:c.765G>A ENSP00000361423.2:p.Glu255=
NM_005157.5:c.708G>A NP_005148.2:p.Glu236=
NM_007313.2:c.765G>A NP_009297.2:p.Glu255=
NM_005157.6:c.708G>A MANE Select NP_005148.2:p.Glu236=
NM_007313.3:c.765G>A NP_009297.2:p.Glu255=