Canonical Allele Identifier: CA1465421088
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754464A= , CM000666.2:g.67754464A= GRCh38
NC_000004.11:g.68620182A= , CM000666.1:g.68620182A= GRCh37
NC_000004.10:g.68302777A= NCBI36
NG_009293.1:g.6623T=

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-129T= NP_000397.1:n.-129T=
NM_001012763.1:c.-129T= NP_001012781.1:n.-129T=