Canonical Allele Identifier: CA467395030
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133748251C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872864C>A , CM000671.2:g.130872864C>A GRCh38
NC_000009.11:g.133748251C>A , CM000671.1:g.133748251C>A GRCh37
NC_000009.10:g.132738072C>A NCBI36
NG_012034.1:g.163984C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.969C>A ENSP00000361423.2:p.Val323=
ENST00000318560.6:c.912C>A MANE Select ENSP00000323315.5:p.Val304=
ENST00000372348.7:c.969C>A ENSP00000361423.2:p.Val323=
ENST00000318560.5:c.912C>A ENSP00000323315.5:p.Val304=
ENST00000372348.6:c.969C>A ENSP00000361423.2:p.Val323=
NM_005157.5:c.912C>A NP_005148.2:p.Val304=
NM_007313.2:c.969C>A NP_009297.2:p.Val323=
NM_005157.6:c.912C>A MANE Select NP_005148.2:p.Val304=
NM_007313.3:c.969C>A NP_009297.2:p.Val323=
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