Canonical Allele Identifier: CA2670820666
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67754436-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754436G>T , CM000666.2:g.67754436G>T GRCh38
NC_000004.11:g.68620154G>T , CM000666.1:g.68620154G>T GRCh37
NC_000004.10:g.68302749G>T NCBI36
NG_009293.1:g.6651C>A

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-101C>A NP_000397.1:n.-101C>A
NM_001012763.1:c.-101C>A NP_001012781.1:n.-101C>A
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