Canonical Allele Identifier: CA1504648248
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.153943626T= , CM000666.2:g.153943626T= GRCh38
NC_000004.11:g.154864778T= , CM000666.1:g.154864778T= GRCh37
NC_000004.10:g.155084228T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741892.1:n.1348-5195T=