Canonical Allele Identifier: CA2670820687
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754475-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754475C>A , CM000666.2:g.67754475C>A GRCh38
NC_000004.11:g.68620193C>A , CM000666.1:g.68620193C>A GRCh37
NC_000004.10:g.68302788C>A NCBI36
NG_009293.1:g.6612G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-140G>T NP_000397.1:n.-140G>T
NM_001012763.1:c.-140G>T NP_001012781.1:n.-140G>T