Canonical Allele Identifier: CA375249980
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133750361G>C (hg19) chr9:g.130874974G>C (hg38)
CIViC: CA375249980
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130874974G>C , CM000671.2:g.130874974G>C GRCh38
NC_000009.11:g.133750361G>C , CM000671.1:g.133750361G>C GRCh37
NC_000009.10:g.132740182G>C NCBI36
NG_012034.1:g.166094G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1249G>C ENSP00000361423.2:p.Gly417Arg
ENST00000318560.6:c.1192G>C MANE Select ENSP00000323315.5:p.Gly398Arg
ENST00000372348.7:c.1249G>C ENSP00000361423.2:p.Gly417Arg
ENST00000318560.5:c.1192G>C ENSP00000323315.5:p.Gly398Arg
ENST00000372348.6:c.1249G>C ENSP00000361423.2:p.Gly417Arg
NM_005157.5:c.1192G>C NP_005148.2:p.Gly398Arg
NM_007313.2:c.1249G>C NP_009297.2:p.Gly417Arg
NM_005157.6:c.1192G>C MANE Select NP_005148.2:p.Gly398Arg
NM_007313.3:c.1249G>C NP_009297.2:p.Gly417Arg
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