Canonical Allele Identifier: CA98672315
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs968319687
gnomAD v2: 4-68620133-T-G
gnomAD v3: 4-67754415-T-G
gnomAD v4: 4-67754415-T-G
MyVariant Identifiers: chr4:g.68620133T>G (hg19) chr4:g.67754415T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754415T>G , CM000666.2:g.67754415T>G GRCh38
NC_000004.11:g.68620133T>G , CM000666.1:g.68620133T>G GRCh37
NC_000004.10:g.68302728T>G NCBI36
NG_009293.1:g.6672A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-80A>C NP_000397.1:n.-80A>C
NM_001012763.1:c.-80A>C NP_001012781.1:n.-80A>C
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