Canonical Allele Identifier: CA2670819648
Gene: GNRHR HGNC NCBI

Linked Data

gnomAD v4: 4-67740193-CA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740196del , CM000666.2:g.67740196del GRCh38
NC_000004.11:g.68605914del , CM000666.1:g.68605914del GRCh37
NC_000004.10:g.68288509del NCBI36
NG_009293.1:g.20893del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*286del MANE Select ENSP00000226413.5:n.*286del
ENST00000226413.4:c.*286del ENSP00000226413.4:n.*286del
NM_000406.2:c.*286del NP_000397.1:n.*286del
NM_001012763.1:c.*395del NP_001012781.1:n.*395del
NM_000406.3:c.*286del MANE Select NP_000397.1:n.*286del
NM_001012763.2:c.*395del NP_001012781.1:n.*395del
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