Canonical Allele Identifier: CA456750116

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100230711T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633088T>C , CM000669.2:g.100633088T>C	GRCh38
NC_000007.13:g.100230711T>C , CM000669.1:g.100230711T>C	GRCh37
NC_000007.12:g.100068647T>C	NCBI36
NG_007989.1:g.13463A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.762A>G MANE Select	ENSP00000223051.3:p.Glu254=
ENST00000223051.7:c.762A>G	ENSP00000223051.3:p.Glu254=
ENST00000431692.5:c.762A>G	ENSP00000413905.1:p.Glu254=
ENST00000462090.5:n.3A>G
ENST00000462107.1:c.762A>G	ENSP00000420525.1:p.Glu254=
ENST00000465294.5:n.767A>G
ENST00000473374.5:n.212A>G
ENST00000473571.1:n.216A>G
ENST00000475011.1:n.291A>G
ENST00000476304.5:n.383A>G
ENST00000490084.5:c.17A>G
NM_001206855.1:c.249A>G	NP_001193784.1:p.Glu83=
NM_003227.3:c.762A>G	NP_003218.2:p.Glu254=
XM_005250553.3:c.762A>G	XP_005250610.1:p.Glu254=
XM_005250554.3:c.762A>G	XP_005250611.1:p.Glu254=
NM_001206855.2:c.249A>G	NP_001193784.1:p.Glu83=
XM_005250553.4:c.762A>G	XP_005250610.1:p.Glu254=
XM_017012573.1:c.762A>G	XP_016868062.1:p.Glu254=
NM_003227.4:c.762A>G MANE Select	NP_003218.2:p.Glu254=
NM_001206855.3:c.249A>G	NP_001193784.1:p.Glu83=