Canonical Allele Identifier: CA98672310

Gene: GNRHR

Linked Data

• dbSNP Id: rs915506197
• gnomAD v4: 4-67754410-C-T
• MyVariant Identifiers: chr4:g.68620128C>T (hg19) ; chr4:g.67754410C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754410C>T , CM000666.2:g.67754410C>T	GRCh38
NC_000004.11:g.68620128C>T , CM000666.1:g.68620128C>T	GRCh37
NC_000004.10:g.68302723C>T	NCBI36
NG_009293.1:g.6677G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-75G>A	NP_000397.1:n.-75G>A
NM_001012763.1:c.-75G>A	NP_001012781.1:n.-75G>A