Canonical Allele Identifier: CA200645311
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1007010398
MyVariant Identifiers: chr9:g.133748006T>C (hg19) chr9:g.130872619T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872619T>C , CM000671.2:g.130872619T>C GRCh38
NC_000009.11:g.133748006T>C , CM000671.1:g.133748006T>C GRCh37
NC_000009.10:g.132737827T>C NCBI36
NG_012034.1:g.163739T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.965-241T>C ENSP00000361423.2:n.965-241T>C
ENST00000318560.6:c.908-241T>C MANE Select ENSP00000323315.5:n.908-241T>C
ENST00000372348.7:c.965-241T>C ENSP00000361423.2:n.965-241T>C
ENST00000318560.5:c.908-241T>C ENSP00000323315.5:n.908-241T>C
ENST00000372348.6:c.965-241T>C ENSP00000361423.2:n.965-241T>C
NM_005157.5:c.908-241T>C NP_005148.2:n.908-241T>C
NM_007313.2:c.965-241T>C NP_009297.2:n.965-241T>C
NM_005157.6:c.908-241T>C MANE Select NP_005148.2:n.908-241T>C
NM_007313.3:c.965-241T>C NP_009297.2:n.965-241T>C
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