Canonical Allele Identifier: CA467395199
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133748401G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130873014G>C , CM000671.2:g.130873014G>C GRCh38
NC_000009.11:g.133748401G>C , CM000671.1:g.133748401G>C GRCh37
NC_000009.10:g.132738222G>C NCBI36
NG_012034.1:g.164134G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000318560.6:c.1062G>C MANE Select ENSP00000323315.5:p.Leu354=
ENST00000372348.7:c.1119G>C ENSP00000361423.2:p.Leu373=
ENST00000318560.5:c.1062G>C ENSP00000323315.5:p.Leu354=
ENST00000372348.6:c.1119G>C ENSP00000361423.2:p.Leu373=
NM_005157.5:c.1062G>C NP_005148.2:p.Leu354=
NM_007313.2:c.1119G>C NP_009297.2:p.Leu373=
NM_005157.6:c.1062G>C MANE Select NP_005148.2:p.Leu354=
NM_007313.3:c.1119G>C NP_009297.2:p.Leu373=