Canonical Allele Identifier: CA163275743

Gene: TFR2

Linked Data

• ClinVar Variation Id: 1077206
• ClinVar RCV Id: RCV001391707
• dbSNP Id: rs946552921
• gnomAD v2: 7-100224421-G-T
• gnomAD v3: 7-100626798-G-T
• gnomAD v4: 7-100626798-G-T
• MyVariant Identifiers: chr7:g.100224421G>T (hg19) ; chr7:g.100626798G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100626798G>T , CM000669.2:g.100626798G>T	GRCh38
NC_000007.13:g.100224421G>T , CM000669.1:g.100224421G>T	GRCh37
NC_000007.12:g.100062357G>T	NCBI36
NG_007989.1:g.19753C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.2101C>A MANE Select	ENSP00000223051.3:p.Arg701=
ENST00000223051.7:c.2101C>A	ENSP00000223051.3:p.Arg701=
ENST00000431692.5:c.*776C>A	ENSP00000413905.1:n.*776C>A
ENST00000461176.1:n.447C>A
ENST00000462090.5:n.1137C>A
ENST00000462107.1:c.2101C>A	ENSP00000420525.1:p.Arg701=
ENST00000465294.5:n.2021C>A
ENST00000476304.5:n.1722C>A
ENST00000490084.5:c.1454C>A
NM_001206855.1:c.1588C>A	NP_001193784.1:p.Arg530=
NM_003227.3:c.2101C>A	NP_003218.2:p.Arg701=
XM_005250553.3:c.2101C>A	XP_005250610.1:p.Arg701=
XM_005250554.3:c.2101C>A	XP_005250611.1:p.Arg701=
XR_927814.1:n.433+4244G>T
NM_001206855.2:c.1588C>A	NP_001193784.1:p.Arg530=
XM_005250553.4:c.2101C>A	XP_005250610.1:p.Arg701=
XM_017012573.1:c.2101C>A	XP_016868062.1:p.Arg701=
NM_003227.4:c.2101C>A MANE Select	NP_003218.2:p.Arg701=
NM_001206855.3:c.1588C>A	NP_001193784.1:p.Arg530=