Canonical Allele Identifier: CA1465421093
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754476T= , CM000666.2:g.67754476T= GRCh38
NC_000004.11:g.68620194T= , CM000666.1:g.68620194T= GRCh37
NC_000004.10:g.68302789T= NCBI36
NG_009293.1:g.6611A=

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-141A= NP_000397.1:n.-141A=
NM_001012763.1:c.-141A= NP_001012781.1:n.-141A=