Canonical Allele Identifier: CA98672355
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs192442227
gnomAD v3: 4-67754482-A-T
gnomAD v4: 4-67754482-A-T
MyVariant Identifiers: chr4:g.68620200A>T (hg19) chr4:g.67754482A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754482A>T , CM000666.2:g.67754482A>T GRCh38
NC_000004.11:g.68620200A>T , CM000666.1:g.68620200A>T GRCh37
NC_000004.10:g.68302795A>T NCBI36
NG_009293.1:g.6605T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-147T>A NP_000397.1:n.-147T>A
NM_001012763.1:c.-147T>A NP_001012781.1:n.-147T>A
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