Canonical Allele Identifier: CA130208
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 16031
dbSNP Id: rs104893843
gnomAD v2: 4-68620024-A-T
gnomAD v3: 4-67754306-A-T
gnomAD v4: 4-67754306-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67754306A>T , CM000666.2:g.67754306A>T GRCh38
NC_000004.11:g.68620024A>T , CM000666.1:g.68620024A>T GRCh37
NC_000004.10:g.68302619A>T NCBI36
NG_009293.1:g.6781T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.30T>A MANE Select ENSP00000226413.5:p.Asn10Lys
ENST00000226413.4:c.30T>A ENSP00000226413.4:p.Asn10Lys
ENST00000420975.2:c.30T>A ENSP00000397561.2:p.Asn10Lys
NM_000406.2:c.30T>A NP_000397.1:p.Asn10Lys
NM_001012763.1:c.30T>A NP_001012781.1:p.Asn10Lys
NM_000406.3:c.30T>A MANE Select NP_000397.1:p.Asn10Lys
NM_001012763.2:c.30T>A NP_001012781.1:p.Asn10Lys