Canonical Allele Identifier: CA200644974
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1034993751
gnomAD v3: 9-130872007-T-A
gnomAD v4: 9-130872007-T-A
MyVariant Identifiers: chr9:g.133747394T>A (hg19) chr9:g.130872007T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872007T>A , CM000671.2:g.130872007T>A GRCh38
NC_000009.11:g.133747394T>A , CM000671.1:g.133747394T>A GRCh37
NC_000009.10:g.132737215T>A NCBI36
NG_012034.1:g.163127T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.880-122T>A ENSP00000361423.2:n.880-122T>A
ENST00000318560.6:c.823-122T>A MANE Select ENSP00000323315.5:n.823-122T>A
ENST00000372348.7:c.880-122T>A ENSP00000361423.2:n.880-122T>A
ENST00000318560.5:c.823-122T>A ENSP00000323315.5:n.823-122T>A
ENST00000372348.6:c.880-122T>A ENSP00000361423.2:n.880-122T>A
NM_005157.5:c.823-122T>A NP_005148.2:n.823-122T>A
NM_007313.2:c.880-122T>A NP_009297.2:n.880-122T>A
NM_005157.6:c.823-122T>A MANE Select NP_005148.2:n.823-122T>A
NM_007313.3:c.880-122T>A NP_009297.2:n.880-122T>A
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