Canonical Allele Identifier: CA98672324

Gene: GNRHR

Linked Data

• dbSNP Id: rs566786665
• gnomAD v2: 4-68620174-C-T
• gnomAD v3: 4-67754456-C-T
• gnomAD v4: 4-67754456-C-T
• MyVariant Identifiers: chr4:g.68620174C>T (hg19) ; chr4:g.67754456C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754456C>T , CM000666.2:g.67754456C>T	GRCh38
NC_000004.11:g.68620174C>T , CM000666.1:g.68620174C>T	GRCh37
NC_000004.10:g.68302769C>T	NCBI36
NG_009293.1:g.6631G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-121G>A	NP_000397.1:n.-121G>A
NM_001012763.1:c.-121G>A	NP_001012781.1:n.-121G>A