Canonical Allele Identifier: CA2762037556
Gene: GNRHR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754447A>T , CM000666.2:g.67754447A>T GRCh38
NC_000004.11:g.68620165A>T , CM000666.1:g.68620165A>T GRCh37
NC_000004.10:g.68302760A>T NCBI36
NG_009293.1:g.6640T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-112T>A NP_000397.1:n.-112T>A
NM_001012763.1:c.-112T>A NP_001012781.1:n.-112T>A