Canonical Allele Identifier: CA552611476

Gene: GNRHR

Linked Data

• dbSNP Id: rs1423298921
• gnomAD v2: 4-68620167-G-A
• gnomAD v3: 4-67754449-G-A
• gnomAD v4: 4-67754449-G-A
• MyVariant Identifiers: chr4:g.68620167G>A (hg19) ; chr4:g.67754449G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754449G>A , CM000666.2:g.67754449G>A	GRCh38
NC_000004.11:g.68620167G>A , CM000666.1:g.68620167G>A	GRCh37
NC_000004.10:g.68302762G>A	NCBI36
NG_009293.1:g.6638C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-114C>T	NP_000397.1:n.-114C>T
NM_001012763.1:c.-114C>T	NP_001012781.1:n.-114C>T