Canonical Allele Identifier: CA797693201
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1189697833
gnomAD v4: 4-67740097-C-T
MyVariant Identifiers: chr4:g.68605815C>T (hg19) chr4:g.67740097C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740097C>T , CM000666.2:g.67740097C>T GRCh38
NC_000004.11:g.68605815C>T , CM000666.1:g.68605815C>T GRCh37
NC_000004.10:g.68288410C>T NCBI36
NG_009293.1:g.20990G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*383G>A MANE Select ENSP00000226413.5:n.*383G>A
ENST00000226413.4:c.*383G>A ENSP00000226413.4:n.*383G>A
NM_000406.2:c.*383G>A NP_000397.1:n.*383G>A
NM_001012763.1:c.*492G>A NP_001012781.1:n.*492G>A
NM_000406.3:c.*383G>A MANE Select NP_000397.1:n.*383G>A
NM_001012763.2:c.*492G>A NP_001012781.1:n.*492G>A
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