Canonical Allele Identifier: CA200645242
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs1056750180
MyVariant Identifiers: chr9:g.130872387G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872387G>A , CM000671.2:g.130872387G>A GRCh38
NC_000009.11:g.133747774G>A , CM000671.1:g.133747774G>A GRCh37
NC_000009.10:g.132737595G>A NCBI36
NG_012034.1:g.163507G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+174G>A ENSP00000361423.2:n.964+174G>A
ENST00000318560.6:c.907+174G>A MANE Select ENSP00000323315.5:n.907+174G>A
ENST00000372348.7:c.964+174G>A ENSP00000361423.2:n.964+174G>A
ENST00000318560.5:c.907+174G>A ENSP00000323315.5:n.907+174G>A
ENST00000372348.6:c.964+174G>A ENSP00000361423.2:n.964+174G>A
NM_005157.5:c.907+174G>A NP_005148.2:n.907+174G>A
NM_007313.2:c.964+174G>A NP_009297.2:n.964+174G>A
NM_005157.6:c.907+174G>A MANE Select NP_005148.2:n.907+174G>A
NM_007313.3:c.964+174G>A NP_009297.2:n.964+174G>A
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