Canonical Allele Identifier: CA200645252
Gene: ABL1 HGNC NCBI

Linked Data

dbSNP Id: rs984185089
gnomAD v2: 9-133747791-T-G
gnomAD v3: 9-130872404-T-G
gnomAD v4: 9-130872404-T-G
MyVariant Identifiers: chr9:g.133747791T>G (hg19) chr9:g.130872404T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872404T>G , CM000671.2:g.130872404T>G GRCh38
NC_000009.11:g.133747791T>G , CM000671.1:g.133747791T>G GRCh37
NC_000009.10:g.132737612T>G NCBI36
NG_012034.1:g.163524T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+191T>G ENSP00000361423.2:n.964+191T>G
ENST00000318560.6:c.907+191T>G MANE Select ENSP00000323315.5:n.907+191T>G
ENST00000372348.7:c.964+191T>G ENSP00000361423.2:n.964+191T>G
ENST00000318560.5:c.907+191T>G ENSP00000323315.5:n.907+191T>G
ENST00000372348.6:c.964+191T>G ENSP00000361423.2:n.964+191T>G
NM_005157.5:c.907+191T>G NP_005148.2:n.907+191T>G
NM_007313.2:c.964+191T>G NP_009297.2:n.964+191T>G
NM_005157.6:c.907+191T>G MANE Select NP_005148.2:n.907+191T>G
NM_007313.3:c.964+191T>G NP_009297.2:n.964+191T>G
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