Canonical Allele Identifier: CA357048166

Gene: GNRHR

Linked Data

• dbSNP Id: rs373245608
• MyVariant Identifiers: chr4:g.68606382A>T (hg19) ; chr4:g.67740664A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740664A>T , CM000666.2:g.67740664A>T	GRCh38
NC_000004.11:g.68606382A>T , CM000666.1:g.68606382A>T	GRCh37
NC_000004.10:g.68288977A>T	NCBI36
NG_009293.1:g.20423T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.803T>A MANE Select	ENSP00000226413.5:p.Met268Lys
ENST00000226413.4:c.803T>A	ENSP00000226413.4:p.Met268Lys
ENST00000420975.2:c.675T>A	ENSP00000397561.2:p.Asn225Lys
NM_000406.2:c.803T>A	NP_000397.1:p.Met268Lys
NM_001012763.1:c.675T>A	NP_001012781.1:p.Asn225Lys
NM_000406.3:c.803T>A MANE Select	NP_000397.1:p.Met268Lys
NM_001012763.2:c.675T>A	NP_001012781.1:p.Asn225Lys