Canonical Allele Identifier: CA1465421092
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754473C= , CM000666.2:g.67754473C= GRCh38
NC_000004.11:g.68620191C= , CM000666.1:g.68620191C= GRCh37
NC_000004.10:g.68302786C= NCBI36
NG_009293.1:g.6614G=

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-138G= NP_000397.1:n.-138G=
NM_001012763.1:c.-138G= NP_001012781.1:n.-138G=