Canonical Allele Identifier: CA797693293
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1433408411
gnomAD v3: 4-67740358-C-A
gnomAD v4: 4-67740358-C-A
MyVariant Identifiers: chr4:g.68606076C>A (hg19) chr4:g.67740358C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740358C>A , CM000666.2:g.67740358C>A GRCh38
NC_000004.11:g.68606076C>A , CM000666.1:g.68606076C>A GRCh37
NC_000004.10:g.68288671C>A NCBI36
NG_009293.1:g.20729G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*122G>T MANE Select ENSP00000226413.5:n.*122G>T
ENST00000226413.4:c.*122G>T ENSP00000226413.4:n.*122G>T
NM_000406.2:c.*122G>T NP_000397.1:n.*122G>T
NM_001012763.1:c.*231G>T NP_001012781.1:n.*231G>T
NM_000406.3:c.*122G>T MANE Select NP_000397.1:n.*122G>T
NM_001012763.2:c.*231G>T NP_001012781.1:n.*231G>T
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