Canonical Allele Identifier: CA2670820650
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754404-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754404A>C , CM000666.2:g.67754404A>C GRCh38
NC_000004.11:g.68620122A>C , CM000666.1:g.68620122A>C GRCh37
NC_000004.10:g.68302717A>C NCBI36
NG_009293.1:g.6683T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-69T>G NP_000397.1:n.-69T>G
NM_001012763.1:c.-69T>G NP_001012781.1:n.-69T>G