Canonical Allele Identifier: CA2670820700
Gene: GNRHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754506dup , CM000666.2:g.67754506dup GRCh38
NC_000004.11:g.68620224dup , CM000666.1:g.68620224dup GRCh37
NC_000004.10:g.68302819dup NCBI36
NG_009293.1:g.6582dup

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-170dup NP_000397.1:n.-170dup
NM_001012763.1:c.-170dup NP_001012781.1:n.-170dup