Canonical Allele Identifier: CA1504648245
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.153943617C= , CM000666.2:g.153943617C= GRCh38
NC_000004.11:g.154864769C= , CM000666.1:g.154864769C= GRCh37
NC_000004.10:g.155084219C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741892.1:n.1348-5204C=