Canonical Allele Identifier: CA439933878

Gene: GNRHR

Linked Data

• MyVariant Identifiers: chr4:g.68619940T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754222T>A , CM000666.2:g.67754222T>A	GRCh38
NC_000004.11:g.68619940T>A , CM000666.1:g.68619940T>A	GRCh37
NC_000004.10:g.68302535T>A	NCBI36
NG_009293.1:g.6865A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.114A>T MANE Select	ENSP00000226413.5:p.Arg38=
ENST00000226413.4:c.114A>T	ENSP00000226413.4:p.Arg38=
ENST00000420975.2:c.114A>T	ENSP00000397561.2:p.Arg38=
NM_000406.2:c.114A>T	NP_000397.1:p.Arg38=
NM_001012763.1:c.114A>T	NP_001012781.1:p.Arg38=
NM_000406.3:c.114A>T MANE Select	NP_000397.1:p.Arg38=
NM_001012763.2:c.114A>T	NP_001012781.1:p.Arg38=