Canonical Allele Identifier: CA797702520
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1404456552
gnomAD v4: 4-67754392-G-A
MyVariant Identifiers: chr4:g.68620110G>A (hg19) chr4:g.67754392G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754392G>A , CM000666.2:g.67754392G>A GRCh38
NC_000004.11:g.68620110G>A , CM000666.1:g.68620110G>A GRCh37
NC_000004.10:g.68302705G>A NCBI36
NG_009293.1:g.6695C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-57C>T NP_000397.1:n.-57C>T
NM_001012763.1:c.-57C>T NP_001012781.1:n.-57C>T
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