Canonical Allele Identifier: CA98672360

Gene: GNRHR

Linked Data

• dbSNP Id: rs898441480
• MyVariant Identifiers: chr4:g.68620252G>T (hg19) ; chr4:g.67754534G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754534G>T , CM000666.2:g.67754534G>T	GRCh38
NC_000004.11:g.68620252G>T , CM000666.1:g.68620252G>T	GRCh37
NC_000004.10:g.68302847G>T	NCBI36
NG_009293.1:g.6553C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-199C>A	NP_000397.1:n.-199C>A
NM_001012763.1:c.-199C>A	NP_001012781.1:n.-199C>A