Canonical Allele Identifier: CA1465421101
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754491G= , CM000666.2:g.67754491G= GRCh38
NC_000004.11:g.68620209G= , CM000666.1:g.68620209G= GRCh37
NC_000004.10:g.68302804G= NCBI36
NG_009293.1:g.6596C=

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-156C= NP_000397.1:n.-156C=
NM_001012763.1:c.-156C= NP_001012781.1:n.-156C=