Canonical Allele Identifier: CA467395044
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133748260G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872873G>C , CM000671.2:g.130872873G>C GRCh38
NC_000009.11:g.133748260G>C , CM000671.1:g.133748260G>C GRCh37
NC_000009.10:g.132738081G>C NCBI36
NG_012034.1:g.163993G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.978G>C ENSP00000361423.2:p.Arg326=
ENST00000318560.6:c.921G>C MANE Select ENSP00000323315.5:p.Arg307=
ENST00000372348.7:c.978G>C ENSP00000361423.2:p.Arg326=
ENST00000318560.5:c.921G>C ENSP00000323315.5:p.Arg307=
ENST00000372348.6:c.978G>C ENSP00000361423.2:p.Arg326=
NM_005157.5:c.921G>C NP_005148.2:p.Arg307=
NM_007313.2:c.978G>C NP_009297.2:p.Arg326=
NM_005157.6:c.921G>C MANE Select NP_005148.2:p.Arg307=
NM_007313.3:c.978G>C NP_009297.2:p.Arg326=
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