Canonical Allele Identifier: CA98667335
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1039843363
gnomAD v3: 4-67740089-A-G
gnomAD v4: 4-67740089-A-G
MyVariant Identifiers: chr4:g.68605807A>G (hg19) chr4:g.67740089A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740089A>G , CM000666.2:g.67740089A>G GRCh38
NC_000004.11:g.68605807A>G , CM000666.1:g.68605807A>G GRCh37
NC_000004.10:g.68288402A>G NCBI36
NG_009293.1:g.20998T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*391T>C MANE Select ENSP00000226413.5:n.*391T>C
ENST00000226413.4:c.*391T>C ENSP00000226413.4:n.*391T>C
NM_000406.2:c.*391T>C NP_000397.1:n.*391T>C
NM_001012763.1:c.*500T>C NP_001012781.1:n.*500T>C
NM_000406.3:c.*391T>C MANE Select NP_000397.1:n.*391T>C
NM_001012763.2:c.*500T>C NP_001012781.1:n.*500T>C
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