Canonical Allele Identifier: CA1063695474
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731934714
gnomAD v3: 4-67754519-A-G
gnomAD v4: 4-67754519-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754519A>G , CM000666.2:g.67754519A>G GRCh38
NC_000004.11:g.68620237A>G , CM000666.1:g.68620237A>G GRCh37
NC_000004.10:g.68302832A>G NCBI36
NG_009293.1:g.6568T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-184T>C NP_000397.1:n.-184T>C
NM_001012763.1:c.-184T>C NP_001012781.1:n.-184T>C