Canonical Allele Identifier: CA1465421090
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754465A= , CM000666.2:g.67754465A= GRCh38
NC_000004.11:g.68620183A= , CM000666.1:g.68620183A= GRCh37
NC_000004.10:g.68302778A= NCBI36
NG_009293.1:g.6622T=

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-130T= NP_000397.1:n.-130T=
NM_001012763.1:c.-130T= NP_001012781.1:n.-130T=