Canonical Allele Identifier: CA2939021
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 904873
ClinVar RCV Id: RCV001153046 RCV001759909
dbSNP Id: rs199976279
ExAC: 4:68620061 C / T
gnomAD v2: 4-68620061-C-T
gnomAD v3: 4-67754343-C-T
gnomAD v4: 4-67754343-C-T
MyVariant Identifiers: chr4:g.68620061C>T (hg19) chr4:g.67754343C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754343C>T , CM000666.2:g.67754343C>T GRCh38
NC_000004.11:g.68620061C>T , CM000666.1:g.68620061C>T GRCh37
NC_000004.10:g.68302656C>T NCBI36
NG_009293.1:g.6744G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.-8G>A MANE Select ENSP00000226413.5:n.-8G>A
ENST00000226413.4:c.-8G>A ENSP00000226413.4:n.-8G>A
NM_000406.2:c.-8G>A NP_000397.1:n.-8G>A
NM_001012763.1:c.-8G>A NP_001012781.1:n.-8G>A
NM_000406.3:c.-8G>A MANE Select NP_000397.1:n.-8G>A
NM_001012763.2:c.-8G>A NP_001012781.1:n.-8G>A
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