Canonical Allele Identifier: CA1504648251
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.153943628G= , CM000666.2:g.153943628G= GRCh38
NC_000004.11:g.154864780G= , CM000666.1:g.154864780G= GRCh37
NC_000004.10:g.155084230G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741892.1:n.1348-5193G=