Canonical Allele Identifier: CA98672305

Gene: GNRHR

Linked Data

• dbSNP Id: rs112702918
• gnomAD v2: 4-68620122-A-G
• gnomAD v3: 4-67754404-A-G
• gnomAD v4: 4-67754404-A-G
• MyVariant Identifiers: chr4:g.68620122A>G (hg19) ; chr4:g.67754404A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754404A>G , CM000666.2:g.67754404A>G	GRCh38
NC_000004.11:g.68620122A>G , CM000666.1:g.68620122A>G	GRCh37
NC_000004.10:g.68302717A>G	NCBI36
NG_009293.1:g.6683T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-69T>C	NP_000397.1:n.-69T>C
NM_001012763.1:c.-69T>C	NP_001012781.1:n.-69T>C