Canonical Allele Identifier: CA2570237122

Gene: FSHR

Linked Data

• gnomAD v4: 2-49154467-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.49154467C>T , CM000664.2:g.49154467C>T	GRCh38
NC_000002.11:g.49381606C>T , CM000664.1:g.49381606C>T	GRCh37
NC_000002.10:g.49235110C>T	NCBI36
NG_008146.1:g.5025G>A , LRG_536:g.5025G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000406846.7:c.-50G>A MANE Select	ENSP00000384708.2:n.-50G>A
ENST00000304421.8:c.-50G>A	ENSP00000306780.4:n.-50G>A
ENST00000406846.6:c.-50G>A	ENSP00000384708.2:n.-50G>A
ENST00000419927.1:c.-50G>A	ENSP00000405775.1:n.-50G>A
NM_000145.3:c.-50G>A , LRG_536t1:c.-50G>A	NP_000136.2:n.-50G>A
NM_181446.2:c.-50G>A	NP_852111.2:n.-50G>A
XM_011532733.1:c.-50G>A	XP_011531035.1:n.-50G>A
XM_011532734.1:c.-634G>A	XP_011531036.1:n.-634G>A
XM_011532737.1:c.-50G>A	XP_011531039.1:n.-50G>A
XM_011532738.1:c.-50G>A	XP_011531040.1:n.-50G>A
XM_011532739.1:c.-50G>A	XP_011531041.1:n.-50G>A
XM_011532740.1:c.-50G>A	XP_011531042.1:n.-50G>A
XM_011532733.2:c.-50G>A	XP_011531035.1:n.-50G>A
XM_011532734.2:c.-634G>A	XP_011531036.1:n.-634G>A
NM_000145.4:c.-50G>A MANE Select	NP_000136.2:n.-50G>A
NM_181446.3:c.-50G>A	NP_852111.2:n.-50G>A