Canonical Allele Identifier: CA163283003

Gene: TFR2

Linked Data

• ClinVar Variation Id: 2002212
• ClinVar RCV Id: RCV002820228
• dbSNP Id: rs1034968542
• gnomAD v4: 7-100633501-G-A
• MyVariant Identifiers: chr7:g.100231124G>A (hg19) ; chr7:g.100633501G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633501G>A , CM000669.2:g.100633501G>A	GRCh38
NC_000007.13:g.100231124G>A , CM000669.1:g.100231124G>A	GRCh37
NC_000007.12:g.100069060G>A	NCBI36
NG_007989.1:g.13050C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.529C>T MANE Select	ENSP00000223051.3:p.Gln177Ter
ENST00000223051.7:c.529C>T	ENSP00000223051.3:p.Gln177Ter
ENST00000431692.5:c.529C>T	ENSP00000413905.1:p.Gln177Ter
ENST00000462107.1:c.529C>T	ENSP00000420525.1:p.Gln177Ter
ENST00000465294.5:n.534C>T
ENST00000475011.1:n.58C>T
ENST00000476304.5:n.150C>T
NM_001206855.1:c.16C>T	NP_001193784.1:p.Gln6Ter
NM_003227.3:c.529C>T	NP_003218.2:p.Gln177Ter
XM_005250553.3:c.529C>T	XP_005250610.1:p.Gln177Ter
XM_005250554.3:c.529C>T	XP_005250611.1:p.Gln177Ter
NM_001206855.2:c.16C>T	NP_001193784.1:p.Gln6Ter
XM_005250553.4:c.529C>T	XP_005250610.1:p.Gln177Ter
XM_017012573.1:c.529C>T	XP_016868062.1:p.Gln177Ter
NM_003227.4:c.529C>T MANE Select	NP_003218.2:p.Gln177Ter
NM_001206855.3:c.16C>T	NP_001193784.1:p.Gln6Ter