Canonical Allele Identifier: CA1465421098
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754483C= , CM000666.2:g.67754483C= GRCh38
NC_000004.11:g.68620201C= , CM000666.1:g.68620201C= GRCh37
NC_000004.10:g.68302796C= NCBI36
NG_009293.1:g.6604G=

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-148G= NP_000397.1:n.-148G=
NM_001012763.1:c.-148G= NP_001012781.1:n.-148G=