Canonical Allele Identifier: CA1515602280
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177298634C= , CM000666.2:g.177298634C= GRCh38
NC_000004.11:g.178219788C= , CM000666.1:g.178219788C= GRCh37
NC_000004.10:g.178456782C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741925.1:n.229+2413G=