Canonical Allele Identifier: CA98672333

Gene: GNRHR

Linked Data

• dbSNP Id: rs939872713
• MyVariant Identifiers: chr4:g.68620191C>T (hg19) ; chr4:g.67754473C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754473C>T , CM000666.2:g.67754473C>T	GRCh38
NC_000004.11:g.68620191C>T , CM000666.1:g.68620191C>T	GRCh37
NC_000004.10:g.68302786C>T	NCBI36
NG_009293.1:g.6614G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-138G>A	NP_000397.1:n.-138G>A
NM_001012763.1:c.-138G>A	NP_001012781.1:n.-138G>A