Canonical Allele Identifier: CA797701389

Gene: GNRHR

Linked Data

• dbSNP Id: rs1223818275
• MyVariant Identifiers: chr4:g.68619381G>A (hg19) ; chr4:g.67753663G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67753663G>A , CM000666.2:g.67753663G>A	GRCh38
NC_000004.11:g.68619381G>A , CM000666.1:g.68619381G>A	GRCh37
NC_000004.10:g.68301976G>A	NCBI36
NG_009293.1:g.7424C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000226413.5:c.522+151C>T MANE Select	ENSP00000226413.5:n.522+151C>T
ENST00000226413.4:c.522+151C>T	ENSP00000226413.4:n.522+151C>T
ENST00000420975.2:c.522+151C>T	ENSP00000397561.2:n.522+151C>T
NM_000406.2:c.522+151C>T	NP_000397.1:n.522+151C>T
NM_001012763.1:c.522+151C>T	NP_001012781.1:n.522+151C>T
XR_938850.1:n.87G>A
NM_000406.3:c.522+151C>T MANE Select	NP_000397.1:n.522+151C>T
NM_001012763.2:c.522+151C>T	NP_001012781.1:n.522+151C>T