Canonical Allele Identifier: CA357048400

Gene: GNRHR

Linked Data

• dbSNP Id: rs375559014
• MyVariant Identifiers: chr4:g.68606408T>C (hg19) ; chr4:g.67740690T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740690T>C , CM000666.2:g.67740690T>C	GRCh38
NC_000004.11:g.68606408T>C , CM000666.1:g.68606408T>C	GRCh37
NC_000004.10:g.68289003T>C	NCBI36
NG_009293.1:g.20397A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.777A>G MANE Select	ENSP00000226413.5:p.Pro259=
ENST00000226413.4:c.777A>G	ENSP00000226413.4:p.Pro259=
ENST00000420975.2:c.649A>G	ENSP00000397561.2:p.Lys217Glu
NM_000406.2:c.777A>G	NP_000397.1:p.Pro259=
NM_001012763.1:c.649A>G	NP_001012781.1:p.Lys217Glu
NM_000406.3:c.777A>G MANE Select	NP_000397.1:p.Pro259=
NM_001012763.2:c.649A>G	NP_001012781.1:p.Lys217Glu