Canonical Allele Identifier: CA2670820677
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754460-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754460T>G , CM000666.2:g.67754460T>G GRCh38
NC_000004.11:g.68620178T>G , CM000666.1:g.68620178T>G GRCh37
NC_000004.10:g.68302773T>G NCBI36
NG_009293.1:g.6627A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-125A>C NP_000397.1:n.-125A>C
NM_001012763.1:c.-125A>C NP_001012781.1:n.-125A>C