Canonical Allele Identifier: CA1465421059
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1577873758
gnomAD v4: 4-67754408-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754408T>C , CM000666.2:g.67754408T>C GRCh38
NC_000004.11:g.68620126T>C , CM000666.1:g.68620126T>C GRCh37
NC_000004.10:g.68302721T>C NCBI36
NG_009293.1:g.6679A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-73A>G NP_000397.1:n.-73A>G
NM_001012763.1:c.-73A>G NP_001012781.1:n.-73A>G