Canonical Allele Identifier: CA1465421802
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs13138607
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67755832G>T , CM000666.2:g.67755832G>T GRCh38
NC_000004.11:g.68621550G>T , CM000666.1:g.68621550G>T GRCh37
NC_000004.10:g.68304145G>T NCBI36
NG_009293.1:g.5255C>A

Transcript Alleles

HGVS Amino-acid change
NM_000406.2:c.-1497C>A NP_000397.1:n.-1497C>A
NM_001012763.1:c.-1497C>A NP_001012781.1:n.-1497C>A
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