Canonical Allele Identifier: CA346817742

Gene: FSHR

Linked Data

• MyVariant Identifiers: chr2:g.49381490A>C (hg19) ; chr2:g.49154351A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.49154351A>C , CM000664.2:g.49154351A>C	GRCh38
NC_000002.11:g.49381490A>C , CM000664.1:g.49381490A>C	GRCh37
NC_000002.10:g.49234994A>C	NCBI36
NG_008146.1:g.5141T>G , LRG_536:g.5141T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000406846.7:c.67T>G MANE Select	ENSP00000384708.2:p.Cys23Gly
ENST00000304421.8:c.67T>G	ENSP00000306780.4:p.Cys23Gly
ENST00000406846.6:c.67T>G	ENSP00000384708.2:p.Cys23Gly
ENST00000419927.1:c.67T>G	ENSP00000405775.1:p.Cys23Gly
ENST00000454032.5:c.67T>G	ENSP00000415504.1:p.Cys23Gly
NM_000145.3:c.67T>G , LRG_536t1:c.67T>G	NP_000136.2:p.Cys23Gly
NM_181446.2:c.67T>G	NP_852111.2:p.Cys23Gly
XM_011532733.1:c.67T>G	XP_011531035.1:p.Cys23Gly
XM_011532734.1:c.-518T>G	XP_011531036.1:n.-518T>G
XM_011532737.1:c.67T>G	XP_011531039.1:p.Cys23Gly
XM_011532738.1:c.67T>G	XP_011531040.1:p.Cys23Gly
XM_011532739.1:c.67T>G	XP_011531041.1:p.Cys23Gly
XM_011532740.1:c.67T>G	XP_011531042.1:p.Cys23Gly
XM_011532733.2:c.67T>G	XP_011531035.1:p.Cys23Gly
XM_011532734.2:c.-518T>G	XP_011531036.1:n.-518T>G
NM_000145.4:c.67T>G MANE Select	NP_000136.2:p.Cys23Gly
NM_181446.3:c.67T>G	NP_852111.2:p.Cys23Gly