Canonical Allele Identifier: CA98672344

Gene: GNRHR

Linked Data

• dbSNP Id: rs1038194837
• gnomAD v4: 4-67754481-T-C
• MyVariant Identifiers: chr4:g.68620199T>C (hg19) ; chr4:g.67754481T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754481T>C , CM000666.2:g.67754481T>C	GRCh38
NC_000004.11:g.68620199T>C , CM000666.1:g.68620199T>C	GRCh37
NC_000004.10:g.68302794T>C	NCBI36
NG_009293.1:g.6606A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-146A>G	NP_000397.1:n.-146A>G
NM_001012763.1:c.-146A>G	NP_001012781.1:n.-146A>G