Canonical Allele Identifier: CA2670820648
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs2109988312
gnomAD v4: 4-67754399-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754399A>G , CM000666.2:g.67754399A>G GRCh38
NC_000004.11:g.68620117A>G , CM000666.1:g.68620117A>G GRCh37
NC_000004.10:g.68302712A>G NCBI36
NG_009293.1:g.6688T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-64T>C NP_000397.1:n.-64T>C
NM_001012763.1:c.-64T>C NP_001012781.1:n.-64T>C