Canonical Allele Identifier: CA98672328

Gene: GNRHR

Linked Data

• dbSNP Id: rs187623180
• gnomAD v2: 4-68620175-G-A
• gnomAD v3: 4-67754457-G-A
• gnomAD v4: 4-67754457-G-A
• MyVariant Identifiers: chr4:g.68620175G>A (hg19) ; chr4:g.68620175_68620185delinsATATGTCAAAT (hg19) ; chr4:g.67754457G>A (hg38) ; chr4:g.67754457_67754467delinsATATGTCAAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754457G>A , CM000666.2:g.67754457G>A	GRCh38
NC_000004.11:g.68620175G>A , CM000666.1:g.68620175G>A	GRCh37
NC_000004.10:g.68302770G>A	NCBI36
NG_009293.1:g.6630C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-122C>T	NP_000397.1:n.-122C>T
NM_001012763.1:c.-122C>T	NP_001012781.1:n.-122C>T