Canonical Allele Identifier: CA1465408699
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1049238675
gnomAD v4: 4-67740132-GT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740139del , CM000666.2:g.67740139del GRCh38
NC_000004.11:g.68605857del , CM000666.1:g.68605857del GRCh37
NC_000004.10:g.68288452del NCBI36
NG_009293.1:g.20954del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*347del MANE Select ENSP00000226413.5:n.*347del
ENST00000226413.4:c.*347del ENSP00000226413.4:n.*347del
NM_000406.2:c.*347del NP_000397.1:n.*347del
NM_001012763.1:c.*456del NP_001012781.1:n.*456del
NM_000406.3:c.*347del MANE Select NP_000397.1:n.*347del
NM_001012763.2:c.*456del NP_001012781.1:n.*456del
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