Canonical Allele Identifier: CA1465421089
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731934074

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754464A>C , CM000666.2:g.67754464A>C GRCh38
NC_000004.11:g.68620182A>C , CM000666.1:g.68620182A>C GRCh37
NC_000004.10:g.68302777A>C NCBI36
NG_009293.1:g.6623T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-129T>G NP_000397.1:n.-129T>G
NM_001012763.1:c.-129T>G NP_001012781.1:n.-129T>G