Canonical Allele Identifier: CA98672320
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs570807794
gnomAD v3: 4-67754426-T-C
gnomAD v4: 4-67754426-T-C
MyVariant Identifiers: chr4:g.68620144T>C (hg19) chr4:g.67754426T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754426T>C , CM000666.2:g.67754426T>C GRCh38
NC_000004.11:g.68620144T>C , CM000666.1:g.68620144T>C GRCh37
NC_000004.10:g.68302739T>C NCBI36
NG_009293.1:g.6661A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-91A>G NP_000397.1:n.-91A>G
NM_001012763.1:c.-91A>G NP_001012781.1:n.-91A>G
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