Canonical Allele Identifier: CA357048356

Gene: GNRHR

Linked Data

• dbSNP Id: rs1339101031
• MyVariant Identifiers: chr4:g.68606403G>C (hg19) ; chr4:g.67740685G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740685G>C , CM000666.2:g.67740685G>C	GRCh38
NC_000004.11:g.68606403G>C , CM000666.1:g.68606403G>C	GRCh37
NC_000004.10:g.68288998G>C	NCBI36
NG_009293.1:g.20402C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.782C>G MANE Select	ENSP00000226413.5:p.Ala261Gly
ENST00000226413.4:c.782C>G	ENSP00000226413.4:p.Ala261Gly
ENST00000420975.2:c.654C>G	ENSP00000397561.2:p.Ser218Arg
NM_000406.2:c.782C>G	NP_000397.1:p.Ala261Gly
NM_001012763.1:c.654C>G	NP_001012781.1:p.Ser218Arg
NM_000406.3:c.782C>G MANE Select	NP_000397.1:p.Ala261Gly
NM_001012763.2:c.654C>G	NP_001012781.1:p.Ser218Arg