Canonical Allele Identifier: CA2938932
Gene: GNRHR HGNC NCBI

Linked Data

ClinVar Variation Id: 904093
ClinVar RCV Id: RCV001151796
dbSNP Id: rs773986790
ExAC: 4:68619589 G / A
gnomAD v2: 4-68619589-G-A
gnomAD v3: 4-67753871-G-A
gnomAD v4: 4-67753871-G-A
MyVariant Identifiers: chr4:g.68619589G>A (hg19) chr4:g.67753871G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753871G>A , CM000666.2:g.67753871G>A GRCh38
NC_000004.11:g.68619589G>A , CM000666.1:g.68619589G>A GRCh37
NC_000004.10:g.68302184G>A NCBI36
NG_009293.1:g.7216C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.465C>T MANE Select ENSP00000226413.5:p.Val155=
ENST00000226413.4:c.465C>T ENSP00000226413.4:p.Val155=
ENST00000420975.2:c.465C>T ENSP00000397561.2:p.Val155=
NM_000406.2:c.465C>T NP_000397.1:p.Val155=
NM_001012763.1:c.465C>T NP_001012781.1:p.Val155=
NM_000406.3:c.465C>T MANE Select NP_000397.1:p.Val155=
NM_001012763.2:c.465C>T NP_001012781.1:p.Val155=
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Search 100 bp 3'