Canonical Allele Identifier: CA200645070
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs910867344
MyVariant Identifiers: chr9:g.133747628G>C (hg19) chr9:g.130872241G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872241G>C , CM000671.2:g.130872241G>C GRCh38
NC_000009.11:g.133747628G>C , CM000671.1:g.133747628G>C GRCh37
NC_000009.10:g.132737449G>C NCBI36
NG_012034.1:g.163361G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+28G>C ENSP00000361423.2:n.964+28G>C
ENST00000318560.6:c.907+28G>C MANE Select ENSP00000323315.5:n.907+28G>C
ENST00000372348.7:c.964+28G>C ENSP00000361423.2:n.964+28G>C
ENST00000318560.5:c.907+28G>C ENSP00000323315.5:n.907+28G>C
ENST00000372348.6:c.964+28G>C ENSP00000361423.2:n.964+28G>C
NM_005157.5:c.907+28G>C NP_005148.2:n.907+28G>C
NM_007313.2:c.964+28G>C NP_009297.2:n.964+28G>C
NM_005157.6:c.907+28G>C MANE Select NP_005148.2:n.907+28G>C
NM_007313.3:c.964+28G>C NP_009297.2:n.964+28G>C
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