Canonical Allele Identifier: CA2670820684
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754468-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754468T>G , CM000666.2:g.67754468T>G GRCh38
NC_000004.11:g.68620186T>G , CM000666.1:g.68620186T>G GRCh37
NC_000004.10:g.68302781T>G NCBI36
NG_009293.1:g.6619A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-133A>C NP_000397.1:n.-133A>C
NM_001012763.1:c.-133A>C NP_001012781.1:n.-133A>C