Canonical Allele Identifier: CA98672358

Gene: GNRHR

Linked Data

• dbSNP Id: rs555925602
• gnomAD v2: 4-68620201-C-T
• gnomAD v3: 4-67754483-C-T
• gnomAD v4: 4-67754483-C-T
• MyVariant Identifiers: chr4:g.68620201C>T (hg19) ; chr4:g.67754483C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754483C>T , CM000666.2:g.67754483C>T	GRCh38
NC_000004.11:g.68620201C>T , CM000666.1:g.68620201C>T	GRCh37
NC_000004.10:g.68302796C>T	NCBI36
NG_009293.1:g.6604G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-148G>A	NP_000397.1:n.-148G>A
NM_001012763.1:c.-148G>A	NP_001012781.1:n.-148G>A