Canonical Allele Identifier: CA646851801
Gene:

Linked Data

COSMIC: COSN10007021
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.773372T>A , CM000664.2:g.773372T>A GRCh38
NC_000002.11:g.773372T>A , CM000664.1:g.773372T>A GRCh37
NC_000002.10:g.763372T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510439.1:c.-24-3464T>A XP_011508741.1:n.-24-3464T>A
XM_011510440.1:c.-24-3464T>A XP_011508742.1:n.-24-3464T>A
XM_011510441.1:c.-24-3464T>A XP_011508743.1:n.-24-3464T>A
XM_011510442.1:c.-24-3464T>A XP_011508744.1:n.-24-3464T>A
XM_011510443.1:c.-24-3464T>A XP_011508745.1:n.-24-3464T>A
XR_922708.1:n.4001-3464T>A
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