Canonical Allele Identifier: CA2670820647
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754393-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754393T>C , CM000666.2:g.67754393T>C GRCh38
NC_000004.11:g.68620111T>C , CM000666.1:g.68620111T>C GRCh37
NC_000004.10:g.68302706T>C NCBI36
NG_009293.1:g.6694A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-58A>G NP_000397.1:n.-58A>G
NM_001012763.1:c.-58A>G NP_001012781.1:n.-58A>G