Canonical Allele Identifier: CA357047957
Gene: GNRHR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.68606359A>T (hg19) chr4:g.67740641A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740641A>T , CM000666.2:g.67740641A>T GRCh38
NC_000004.11:g.68606359A>T , CM000666.1:g.68606359A>T GRCh37
NC_000004.10:g.68288954A>T NCBI36
NG_009293.1:g.20446T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.826T>A MANE Select ENSP00000226413.5:p.Phe276Ile
ENST00000226413.4:c.826T>A ENSP00000226413.4:p.Phe276Ile
ENST00000420975.2:c.698T>A ENSP00000397561.2:p.Ile233Asn
NM_000406.2:c.826T>A NP_000397.1:p.Phe276Ile
NM_001012763.1:c.698T>A NP_001012781.1:p.Ile233Asn
NM_000406.3:c.826T>A MANE Select NP_000397.1:p.Phe276Ile
NM_001012763.2:c.698T>A NP_001012781.1:p.Ile233Asn
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