Canonical Allele Identifier: CA357054299

Gene: GNRHR

Linked Data

• MyVariant Identifiers: chr4:g.68619545A>G (hg19) ; chr4:g.67753827A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753827A>G , CM000666.2:g.67753827A>G	GRCh38
NC_000004.11:g.68619545A>G , CM000666.1:g.68619545A>G	GRCh37
NC_000004.10:g.68302140A>G	NCBI36
NG_009293.1:g.7260T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.509T>C MANE Select	ENSP00000226413.5:p.Phe170Ser
ENST00000226413.4:c.509T>C	ENSP00000226413.4:p.Phe170Ser
ENST00000420975.2:c.509T>C	ENSP00000397561.2:p.Phe170Ser
NM_000406.2:c.509T>C	NP_000397.1:p.Phe170Ser
NM_001012763.1:c.509T>C	NP_001012781.1:p.Phe170Ser
NM_000406.3:c.509T>C MANE Select	NP_000397.1:p.Phe170Ser
NM_001012763.2:c.509T>C	NP_001012781.1:p.Phe170Ser