Canonical Allele Identifier: CA467395116
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133748321A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872934A>C , CM000671.2:g.130872934A>C GRCh38
NC_000009.11:g.133748321A>C , CM000671.1:g.133748321A>C GRCh37
NC_000009.10:g.132738142A>C NCBI36
NG_012034.1:g.164054A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372348.9:c.1039A>C ENSP00000361423.2:p.Arg347=
ENST00000318560.6:c.982A>C MANE Select ENSP00000323315.5:p.Arg328=
ENST00000372348.7:c.1039A>C ENSP00000361423.2:p.Arg347=
ENST00000318560.5:c.982A>C ENSP00000323315.5:p.Arg328=
ENST00000372348.6:c.1039A>C ENSP00000361423.2:p.Arg347=
NM_005157.5:c.982A>C NP_005148.2:p.Arg328=
NM_007313.2:c.1039A>C NP_009297.2:p.Arg347=
NM_005157.6:c.982A>C MANE Select NP_005148.2:p.Arg328=
NM_007313.3:c.1039A>C NP_009297.2:p.Arg347=
Search 100 bp 5'
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