Canonical Allele Identifier: CA439930439

Gene: GNRHR

Linked Data

• MyVariant Identifiers: chr4:g.68619604T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753886T>C , CM000666.2:g.67753886T>C	GRCh38
NC_000004.11:g.68619604T>C , CM000666.1:g.68619604T>C	GRCh37
NC_000004.10:g.68302199T>C	NCBI36
NG_009293.1:g.7201A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.450A>G MANE Select	ENSP00000226413.5:p.Lys150=
ENST00000226413.4:c.450A>G	ENSP00000226413.4:p.Lys150=
ENST00000420975.2:c.450A>G	ENSP00000397561.2:p.Lys150=
NM_000406.2:c.450A>G	NP_000397.1:p.Lys150=
NM_001012763.1:c.450A>G	NP_001012781.1:p.Lys150=
NM_000406.3:c.450A>G MANE Select	NP_000397.1:p.Lys150=
NM_001012763.2:c.450A>G	NP_001012781.1:p.Lys150=