Canonical Allele Identifier: CA10621570
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 349457
ClinVar RCV Id: RCV000357929 RCV001672645
dbSNP Id: rs2627261
gnomAD v2: 4-68620115-C-T
gnomAD v3: 4-67754397-C-T
gnomAD v4: 4-67754397-C-T
MyVariant Identifiers: chr4:g.68620115C>T (hg19) chr4:g.67754397C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754397C>T , CM000666.2:g.67754397C>T GRCh38
NC_000004.11:g.68620115C>T , CM000666.1:g.68620115C>T GRCh37
NC_000004.10:g.68302710C>T NCBI36
NG_009293.1:g.6690G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000406.2:c.-62G>A NP_000397.1:n.-62G>A
NM_001012763.1:c.-62G>A NP_001012781.1:n.-62G>A
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