Canonical Allele Identifier: CA375249338
Gene: ABL1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133748245A>T (hg19) chr9:g.130872858A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872858A>T , CM000671.2:g.130872858A>T GRCh38
NC_000009.11:g.133748245A>T , CM000671.1:g.133748245A>T GRCh37
NC_000009.10:g.132738066A>T NCBI36
NG_012034.1:g.163978A>T

Transcript Alleles

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