Canonical Allele Identifier: CA357048523

Gene: GNRHR

Linked Data

• gnomAD v4: 4-67740713-T-A
• MyVariant Identifiers: chr4:g.68606431T>A (hg19) ; chr4:g.67740713T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67740713T>A , CM000666.2:g.67740713T>A	GRCh38
NC_000004.11:g.68606431T>A , CM000666.1:g.68606431T>A	GRCh37
NC_000004.10:g.68289026T>A	NCBI36
NG_009293.1:g.20374A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.754A>T MANE Select	ENSP00000226413.5:p.Asn252Tyr
ENST00000226413.4:c.754A>T	ENSP00000226413.4:p.Asn252Tyr
ENST00000420975.2:c.626A>T	ENSP00000397561.2:p.Glu209Val
NM_000406.2:c.754A>T	NP_000397.1:p.Asn252Tyr
NM_001012763.1:c.626A>T	NP_001012781.1:p.Glu209Val
NM_000406.3:c.754A>T MANE Select	NP_000397.1:p.Asn252Tyr
NM_001012763.2:c.626A>T	NP_001012781.1:p.Glu209Val