Canonical Allele Identifier: CA1063695444
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731932863
gnomAD v3: 4-67754405-A-G
gnomAD v4: 4-67754405-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754405A>G , CM000666.2:g.67754405A>G GRCh38
NC_000004.11:g.68620123A>G , CM000666.1:g.68620123A>G GRCh37
NC_000004.10:g.68302718A>G NCBI36
NG_009293.1:g.6682T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-70T>C NP_000397.1:n.-70T>C
NM_001012763.1:c.-70T>C NP_001012781.1:n.-70T>C
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