Canonical Allele Identifier: CA1465421078
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731933662

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754452del , CM000666.2:g.67754452del GRCh38
NC_000004.11:g.68620170del , CM000666.1:g.68620170del GRCh37
NC_000004.10:g.68302765del NCBI36
NG_009293.1:g.6637del

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-115del NP_000397.1:n.-115del
NM_001012763.1:c.-115del NP_001012781.1:n.-115del