Canonical Allele Identifier: CA346817732

Gene: FSHR

Linked Data

• MyVariant Identifiers: chr2:g.49381486T>C (hg19) ; chr2:g.49154347T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.49154347T>C , CM000664.2:g.49154347T>C	GRCh38
NC_000002.11:g.49381486T>C , CM000664.1:g.49381486T>C	GRCh37
NC_000002.10:g.49234990T>C	NCBI36
NG_008146.1:g.5145A>G , LRG_536:g.5145A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000406846.7:c.71A>G MANE Select	ENSP00000384708.2:p.His24Arg
ENST00000304421.8:c.71A>G	ENSP00000306780.4:p.His24Arg
ENST00000406846.6:c.71A>G	ENSP00000384708.2:p.His24Arg
ENST00000419927.1:c.71A>G	ENSP00000405775.1:p.His24Arg
ENST00000454032.5:c.71A>G	ENSP00000415504.1:p.His24Arg
NM_000145.3:c.71A>G , LRG_536t1:c.71A>G	NP_000136.2:p.His24Arg
NM_181446.2:c.71A>G	NP_852111.2:p.His24Arg
XM_011532733.1:c.71A>G	XP_011531035.1:p.His24Arg
XM_011532734.1:c.-514A>G	XP_011531036.1:n.-514A>G
XM_011532737.1:c.71A>G	XP_011531039.1:p.His24Arg
XM_011532738.1:c.71A>G	XP_011531040.1:p.His24Arg
XM_011532739.1:c.71A>G	XP_011531041.1:p.His24Arg
XM_011532740.1:c.71A>G	XP_011531042.1:p.His24Arg
XM_011532733.2:c.71A>G	XP_011531035.1:p.His24Arg
XM_011532734.2:c.-514A>G	XP_011531036.1:n.-514A>G
NM_000145.4:c.71A>G MANE Select	NP_000136.2:p.His24Arg
NM_181446.3:c.71A>G	NP_852111.2:p.His24Arg