Canonical Allele Identifier: CA1465421105
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731934622
gnomAD v4: 4-67754502-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754502G>A , CM000666.2:g.67754502G>A GRCh38
NC_000004.11:g.68620220G>A , CM000666.1:g.68620220G>A GRCh37
NC_000004.10:g.68302815G>A NCBI36
NG_009293.1:g.6585C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-167C>T NP_000397.1:n.-167C>T
NM_001012763.1:c.-167C>T NP_001012781.1:n.-167C>T
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