Canonical Allele Identifier: CA439928993

Gene: GNRHR

Linked Data

• MyVariant Identifiers: chr4:g.68619559G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753841G>A , CM000666.2:g.67753841G>A	GRCh38
NC_000004.11:g.68619559G>A , CM000666.1:g.68619559G>A	GRCh37
NC_000004.10:g.68302154G>A	NCBI36
NG_009293.1:g.7246C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000226413.5:c.495C>T MANE Select	ENSP00000226413.5:p.Ile165=
ENST00000226413.4:c.495C>T	ENSP00000226413.4:p.Ile165=
ENST00000420975.2:c.495C>T	ENSP00000397561.2:p.Ile165=
NM_000406.2:c.495C>T	NP_000397.1:p.Ile165=
NM_001012763.1:c.495C>T	NP_001012781.1:p.Ile165=
NM_000406.3:c.495C>T MANE Select	NP_000397.1:p.Ile165=
NM_001012763.2:c.495C>T	NP_001012781.1:p.Ile165=