Canonical Allele Identifier: CA2692152530
Gene: ABL1 HGNC NCBI

Linked Data

gnomAD v4: 9-130872245-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.130872245C>T , CM000671.2:g.130872245C>T GRCh38
NC_000009.11:g.133747632C>T , CM000671.1:g.133747632C>T GRCh37
NC_000009.10:g.132737453C>T NCBI36
NG_012034.1:g.163365C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372348.9:c.964+32C>T ENSP00000361423.2:n.964+32C>T
ENST00000318560.6:c.907+32C>T MANE Select ENSP00000323315.5:n.907+32C>T
ENST00000372348.7:c.964+32C>T ENSP00000361423.2:n.964+32C>T
ENST00000318560.5:c.907+32C>T ENSP00000323315.5:n.907+32C>T
ENST00000372348.6:c.964+32C>T ENSP00000361423.2:n.964+32C>T
NM_005157.5:c.907+32C>T NP_005148.2:n.907+32C>T
NM_007313.2:c.964+32C>T NP_009297.2:n.964+32C>T
NM_005157.6:c.907+32C>T MANE Select NP_005148.2:n.907+32C>T
NM_007313.3:c.964+32C>T NP_009297.2:n.964+32C>T
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