Canonical Allele Identifier: CA797702585

Gene: GNRHR

Linked Data

• dbSNP Id: rs1331449115
• gnomAD v3: 4-67754460-T-C
• gnomAD v4: 4-67754460-T-C
• MyVariant Identifiers: chr4:g.68620178T>C (hg19) ; chr4:g.67754460T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754460T>C , CM000666.2:g.67754460T>C	GRCh38
NC_000004.11:g.68620178T>C , CM000666.1:g.68620178T>C	GRCh37
NC_000004.10:g.68302773T>C	NCBI36
NG_009293.1:g.6627A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-125A>G	NP_000397.1:n.-125A>G
NM_001012763.1:c.-125A>G	NP_001012781.1:n.-125A>G