Canonical Allele Identifier: CA1465421071
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754437G= , CM000666.2:g.67754437G= GRCh38
NC_000004.11:g.68620155G= , CM000666.1:g.68620155G= GRCh37
NC_000004.10:g.68302750G= NCBI36
NG_009293.1:g.6650C=

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-102C= NP_000397.1:n.-102C=
NM_001012763.1:c.-102C= NP_001012781.1:n.-102C=