Canonical Allele Identifier: CA797702545
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1426815995
gnomAD v3: 4-67754437-G-C
gnomAD v4: 4-67754437-G-C
MyVariant Identifiers: chr4:g.68620155G>C (hg19) chr4:g.67754437G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754437G>C , CM000666.2:g.67754437G>C GRCh38
NC_000004.11:g.68620155G>C , CM000666.1:g.68620155G>C GRCh37
NC_000004.10:g.68302750G>C NCBI36
NG_009293.1:g.6650C>G

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-102C>G NP_000397.1:n.-102C>G
NM_001012763.1:c.-102C>G NP_001012781.1:n.-102C>G
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