Canonical Allele Identifier: CA1465421065
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754416T= , CM000666.2:g.67754416T= GRCh38
NC_000004.11:g.68620134T= , CM000666.1:g.68620134T= GRCh37
NC_000004.10:g.68302729T= NCBI36
NG_009293.1:g.6671A=

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-81A= NP_000397.1:n.-81A=
NM_001012763.1:c.-81A= NP_001012781.1:n.-81A=