Canonical Allele Identifier: CA2938928
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs770238666
ExAC: 4:68619558 G / A
gnomAD v2: 4-68619558-G-A
gnomAD v4: 4-67753840-G-A
MyVariant Identifiers: chr4:g.68619558G>A (hg19) chr4:g.67753840G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67753840G>A , CM000666.2:g.67753840G>A GRCh38
NC_000004.11:g.68619558G>A , CM000666.1:g.68619558G>A GRCh37
NC_000004.10:g.68302153G>A NCBI36
NG_009293.1:g.7247C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000226413.5:c.496C>T MANE Select ENSP00000226413.5:p.Leu166Phe
ENST00000226413.4:c.496C>T ENSP00000226413.4:p.Leu166Phe
ENST00000420975.2:c.496C>T ENSP00000397561.2:p.Leu166Phe
NM_000406.2:c.496C>T NP_000397.1:p.Leu166Phe
NM_001012763.1:c.496C>T NP_001012781.1:p.Leu166Phe
NM_000406.3:c.496C>T MANE Select NP_000397.1:p.Leu166Phe
NM_001012763.2:c.496C>T NP_001012781.1:p.Leu166Phe
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