Canonical Allele Identifier: CA2670820699
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754503-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754503T>C , CM000666.2:g.67754503T>C GRCh38
NC_000004.11:g.68620221T>C , CM000666.1:g.68620221T>C GRCh37
NC_000004.10:g.68302816T>C NCBI36
NG_009293.1:g.6584A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-168A>G NP_000397.1:n.-168A>G
NM_001012763.1:c.-168A>G NP_001012781.1:n.-168A>G