Canonical Allele Identifier: CA797702588

Gene: GNRHR

Linked Data

• dbSNP Id: rs1281674891
• gnomAD v3: 4-67754465-A-G
• gnomAD v4: 4-67754465-A-G
• MyVariant Identifiers: chr4:g.68620183A>G (hg19) ; chr4:g.67754465A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754465A>G , CM000666.2:g.67754465A>G	GRCh38
NC_000004.11:g.68620183A>G , CM000666.1:g.68620183A>G	GRCh37
NC_000004.10:g.68302778A>G	NCBI36
NG_009293.1:g.6622T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-130T>C	NP_000397.1:n.-130T>C
NM_001012763.1:c.-130T>C	NP_001012781.1:n.-130T>C