Canonical Allele Identifier: CA375249587
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133748363T>C (hg19) chr9:g.130872976T>C (hg38)
CIViC: CA375249587
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872976T>C , CM000671.2:g.130872976T>C GRCh38
NC_000009.11:g.133748363T>C , CM000671.1:g.133748363T>C GRCh37
NC_000009.10:g.132738184T>C NCBI36
NG_012034.1:g.164096T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1081T>C ENSP00000361423.2:p.Tyr361His
ENST00000318560.6:c.1024T>C MANE Select ENSP00000323315.5:p.Tyr342His
ENST00000372348.7:c.1081T>C ENSP00000361423.2:p.Tyr361His
ENST00000318560.5:c.1024T>C ENSP00000323315.5:p.Tyr342His
ENST00000372348.6:c.1081T>C ENSP00000361423.2:p.Tyr361His
NM_005157.5:c.1024T>C NP_005148.2:p.Tyr342His
NM_007313.2:c.1081T>C NP_009297.2:p.Tyr361His
NM_005157.6:c.1024T>C MANE Select NP_005148.2:p.Tyr342His
NM_007313.3:c.1081T>C NP_009297.2:p.Tyr361His
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