Canonical Allele Identifier: CA456750000

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100230689T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633066T>G , CM000669.2:g.100633066T>G	GRCh38
NC_000007.13:g.100230689T>G , CM000669.1:g.100230689T>G	GRCh37
NC_000007.12:g.100068625T>G	NCBI36
NG_007989.1:g.13485A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.784A>C MANE Select	ENSP00000223051.3:p.Arg262=
ENST00000223051.7:c.784A>C	ENSP00000223051.3:p.Arg262=
ENST00000431692.5:c.784A>C	ENSP00000413905.1:p.Arg262=
ENST00000462090.5:n.25A>C
ENST00000462107.1:c.784A>C	ENSP00000420525.1:p.Arg262=
ENST00000465294.5:n.789A>C
ENST00000473374.5:n.234A>C
ENST00000473571.1:n.238A>C
ENST00000475011.1:n.313A>C
ENST00000476304.5:n.405A>C
ENST00000490084.5:c.39A>C
NM_001206855.1:c.271A>C	NP_001193784.1:p.Arg91=
NM_003227.3:c.784A>C	NP_003218.2:p.Arg262=
XM_005250553.3:c.784A>C	XP_005250610.1:p.Arg262=
XM_005250554.3:c.784A>C	XP_005250611.1:p.Arg262=
NM_001206855.2:c.271A>C	NP_001193784.1:p.Arg91=
XM_005250553.4:c.784A>C	XP_005250610.1:p.Arg262=
XM_017012573.1:c.784A>C	XP_016868062.1:p.Arg262=
NM_003227.4:c.784A>C MANE Select	NP_003218.2:p.Arg262=
NM_001206855.3:c.271A>C	NP_001193784.1:p.Arg91=