Canonical Allele Identifier: CA2670820660
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754427-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754427T>A , CM000666.2:g.67754427T>A GRCh38
NC_000004.11:g.68620145T>A , CM000666.1:g.68620145T>A GRCh37
NC_000004.10:g.68302740T>A NCBI36
NG_009293.1:g.6660A>T

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-92A>T NP_000397.1:n.-92A>T
NM_001012763.1:c.-92A>T NP_001012781.1:n.-92A>T
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