Canonical Allele Identifier: CA1465421026

Gene: GNRHR

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67754347A= , CM000666.2:g.67754347A=	GRCh38
NC_000004.11:g.68620065A= , CM000666.1:g.68620065A=	GRCh37
NC_000004.10:g.68302660A=	NCBI36
NG_009293.1:g.6740T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.-12T= MANE Select	ENSP00000226413.5:n.-12T=
ENST00000226413.4:c.-12T=	ENSP00000226413.4:n.-12T=
NM_000406.2:c.-12T=	NP_000397.1:n.-12T=
NM_001012763.1:c.-12T=	NP_001012781.1:n.-12T=
NM_000406.3:c.-12T= MANE Select	NP_000397.1:n.-12T=
NM_001012763.2:c.-12T=	NP_001012781.1:n.-12T=