Canonical Allele Identifier: CA1468682097
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74554034C= , CM000666.2:g.74554034C= GRCh38
NC_000004.11:g.75419751C= , CM000666.1:g.75419751C= GRCh37
NC_000004.10:g.75638615C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741513.1:n.167-1202G=