Canonical Allele Identifier: CA797693259
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1159161292
MyVariant Identifiers: chr4:g.68605992del (hg19) chr4:g.67740274del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740275del , CM000666.2:g.67740275del GRCh38
NC_000004.11:g.68605993del , CM000666.1:g.68605993del GRCh37
NC_000004.10:g.68288588del NCBI36
NG_009293.1:g.20813del

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*206del MANE Select ENSP00000226413.5:n.*206del
ENST00000226413.4:c.*206del ENSP00000226413.4:n.*206del
NM_000406.2:c.*206del NP_000397.1:n.*206del
NM_001012763.1:c.*315del NP_001012781.1:n.*315del
NM_000406.3:c.*206del MANE Select NP_000397.1:n.*206del
NM_001012763.2:c.*315del NP_001012781.1:n.*315del
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