Canonical Allele Identifier: CA650202937
Gene:

Linked Data

COSMIC: COSN15260558
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113661122T>C , CM000667.2:g.113661122T>C GRCh38
NC_000005.9:g.112996819T>C , CM000667.1:g.112996819T>C GRCh37
NC_000005.8:g.113024718T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27758T>C
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