Canonical Allele Identifier: CA1480021966
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99474319C= , CM000666.2:g.99474319C= GRCh38
NC_000004.11:g.100395476C= , CM000666.1:g.100395476C= GRCh37
NC_000004.10:g.100614499C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506494.1:n.242+2429G=