Canonical Allele Identifier: CA357047279
Gene: GNRHR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740523T>A , CM000666.2:g.67740523T>A GRCh38
NC_000004.11:g.68606241T>A , CM000666.1:g.68606241T>A GRCh37
NC_000004.10:g.68288836T>A NCBI36
NG_009293.1:g.20564A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.944A>T MANE Select ENSP00000226413.5:p.Asn315Ile
ENST00000226413.4:c.944A>T ENSP00000226413.4:p.Asn315Ile
ENST00000420975.2:c.816A>T ENSP00000397561.2:n.816A>T
NM_000406.2:c.944A>T NP_000397.1:p.Asn315Ile
NM_001012763.1:c.*66A>T NP_001012781.1:n.*66A>T
NM_000406.3:c.944A>T MANE Select NP_000397.1:p.Asn315Ile
NM_001012763.2:c.*66A>T NP_001012781.1:n.*66A>T