Canonical Allele Identifier: CA467395195
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133748399C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873012C>T , CM000671.2:g.130873012C>T GRCh38
NC_000009.11:g.133748399C>T , CM000671.1:g.133748399C>T GRCh37
NC_000009.10:g.132738220C>T NCBI36
NG_012034.1:g.164132C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1117C>T ENSP00000361423.2:p.Leu373=
ENST00000318560.6:c.1060C>T MANE Select ENSP00000323315.5:p.Leu354=
ENST00000372348.7:c.1117C>T ENSP00000361423.2:p.Leu373=
ENST00000318560.5:c.1060C>T ENSP00000323315.5:p.Leu354=
ENST00000372348.6:c.1117C>T ENSP00000361423.2:p.Leu373=
NM_005157.5:c.1060C>T NP_005148.2:p.Leu354=
NM_007313.2:c.1117C>T NP_009297.2:p.Leu373=
NM_005157.6:c.1060C>T MANE Select NP_005148.2:p.Leu354=
NM_007313.3:c.1117C>T NP_009297.2:p.Leu373=