Canonical Allele Identifier: CA1504648256
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.153943634C= , CM000666.2:g.153943634C= GRCh38
NC_000004.11:g.154864786C= , CM000666.1:g.154864786C= GRCh37
NC_000004.10:g.155084236C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741892.1:n.1348-5187C=