Canonical Allele Identifier: CA552611479

Gene: GNRHR

Linked Data

• dbSNP Id: rs1326907363
• gnomAD v2: 4-68620196-A-G
• gnomAD v3: 4-67754478-A-G
• gnomAD v4: 4-67754478-A-G
• MyVariant Identifiers: chr4:g.68620196A>G (hg19) ; chr4:g.67754478A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754478A>G , CM000666.2:g.67754478A>G	GRCh38
NC_000004.11:g.68620196A>G , CM000666.1:g.68620196A>G	GRCh37
NC_000004.10:g.68302791A>G	NCBI36
NG_009293.1:g.6609T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000406.2:c.-143T>C	NP_000397.1:n.-143T>C
NM_001012763.1:c.-143T>C	NP_001012781.1:n.-143T>C