Canonical Allele Identifier: CA426097876

Gene: FSHR

Linked Data

• MyVariant Identifiers: chr2:g.49381491G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.49154352G>A , CM000664.2:g.49154352G>A	GRCh38
NC_000002.11:g.49381491G>A , CM000664.1:g.49381491G>A	GRCh37
NC_000002.10:g.49234995G>A	NCBI36
NG_008146.1:g.5140C>T , LRG_536:g.5140C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000406846.7:c.66C>T MANE Select	ENSP00000384708.2:p.Ile22=
ENST00000304421.8:c.66C>T	ENSP00000306780.4:p.Ile22=
ENST00000406846.6:c.66C>T	ENSP00000384708.2:p.Ile22=
ENST00000419927.1:c.66C>T	ENSP00000405775.1:p.Ile22=
ENST00000454032.5:c.66C>T	ENSP00000415504.1:p.Ile22=
NM_000145.3:c.66C>T , LRG_536t1:c.66C>T	NP_000136.2:p.Ile22=
NM_181446.2:c.66C>T	NP_852111.2:p.Ile22=
XM_011532733.1:c.66C>T	XP_011531035.1:p.Ile22=
XM_011532734.1:c.-519C>T	XP_011531036.1:n.-519C>T
XM_011532737.1:c.66C>T	XP_011531039.1:p.Ile22=
XM_011532738.1:c.66C>T	XP_011531040.1:p.Ile22=
XM_011532739.1:c.66C>T	XP_011531041.1:p.Ile22=
XM_011532740.1:c.66C>T	XP_011531042.1:p.Ile22=
XM_011532733.2:c.66C>T	XP_011531035.1:p.Ile22=
XM_011532734.2:c.-519C>T	XP_011531036.1:n.-519C>T
NM_000145.4:c.66C>T MANE Select	NP_000136.2:p.Ile22=
NM_181446.3:c.66C>T	NP_852111.2:p.Ile22=