Canonical Allele Identifier: CA456749269

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100224455C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100626832C>G , CM000669.2:g.100626832C>G	GRCh38
NC_000007.13:g.100224455C>G , CM000669.1:g.100224455C>G	GRCh37
NC_000007.12:g.100062391C>G	NCBI36
NG_007989.1:g.19719G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000223051.8:c.2067G>C MANE Select	ENSP00000223051.3:p.Arg689=
ENST00000223051.7:c.2067G>C	ENSP00000223051.3:p.Arg689=
ENST00000431692.5:c.*742G>C	ENSP00000413905.1:n.*742G>C
ENST00000461176.1:n.413G>C
ENST00000462090.5:n.1103G>C
ENST00000462107.1:c.2067G>C	ENSP00000420525.1:p.Arg689=
ENST00000465294.5:n.1987G>C
ENST00000476304.5:n.1688G>C
ENST00000490084.5:c.1420G>C
NM_001206855.1:c.1554G>C	NP_001193784.1:p.Arg518=
NM_003227.3:c.2067G>C	NP_003218.2:p.Arg689=
XM_005250553.3:c.2067G>C	XP_005250610.1:p.Arg689=
XM_005250554.3:c.2067G>C	XP_005250611.1:p.Arg689=
XR_927814.1:n.433+4278C>G
NM_001206855.2:c.1554G>C	NP_001193784.1:p.Arg518=
XM_005250553.4:c.2067G>C	XP_005250610.1:p.Arg689=
XM_017012573.1:c.2067G>C	XP_016868062.1:p.Arg689=
NM_003227.4:c.2067G>C MANE Select	NP_003218.2:p.Arg689=
NM_001206855.3:c.1554G>C	NP_001193784.1:p.Arg518=