Canonical Allele Identifier: CA1465421799
Community Standard Title: NC_000004.12:g.67755832G=
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67755832G= , CM000666.2:g.67755832G= GRCh38
NC_000004.11:g.68621550G= , CM000666.1:g.68621550G= GRCh37
NC_000004.10:g.68304145G= NCBI36
NG_009293.1:g.5255C=

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-1497C= NP_000397.1:n.-1497C=
NM_001012763.1:c.-1497C= NP_001012781.1:n.-1497C=