Canonical Allele Identifier: CA1465421081
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs566786665
gnomAD v4: 4-67754456-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754456C>A , CM000666.2:g.67754456C>A GRCh38
NC_000004.11:g.68620174C>A , CM000666.1:g.68620174C>A GRCh37
NC_000004.10:g.68302769C>A NCBI36
NG_009293.1:g.6631G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-121G>T NP_000397.1:n.-121G>T
NM_001012763.1:c.-121G>T NP_001012781.1:n.-121G>T