Canonical Allele Identifier: CA2573141352

Gene: TFR2

Linked Data

• ClinVar Variation Id: 1643097
• ClinVar RCV Id: RCV002135864
• dbSNP Id: rs2131320575

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633344G>C , CM000669.2:g.100633344G>C	GRCh38
NC_000007.13:g.100230967G>C , CM000669.1:g.100230967G>C	GRCh37
NC_000007.12:g.100068903G>C	NCBI36
NG_007989.1:g.13207C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.615-4C>G MANE Select	ENSP00000223051.3:n.615-4C>G
ENST00000223051.7:c.615-4C>G	ENSP00000223051.3:n.615-4C>G
ENST00000431692.5:c.615-4C>G	ENSP00000413905.1:n.615-4C>G
ENST00000462107.1:c.615-4C>G	ENSP00000420525.1:n.615-4C>G
ENST00000465294.5:n.620-4C>G
ENST00000473374.5:n.61C>G
ENST00000473571.1:n.65C>G
ENST00000475011.1:n.144-4C>G
ENST00000476304.5:n.236-4C>G
NM_001206855.1:c.102-4C>G	NP_001193784.1:n.102-4C>G
NM_003227.3:c.615-4C>G	NP_003218.2:n.615-4C>G
XM_005250553.3:c.615-4C>G	XP_005250610.1:n.615-4C>G
XM_005250554.3:c.615-4C>G	XP_005250611.1:n.615-4C>G
NM_001206855.2:c.102-4C>G	NP_001193784.1:n.102-4C>G
XM_005250553.4:c.615-4C>G	XP_005250610.1:n.615-4C>G
XM_017012573.1:c.615-4C>G	XP_016868062.1:n.615-4C>G
NM_003227.4:c.615-4C>G MANE Select	NP_003218.2:n.615-4C>G
NM_001206855.3:c.102-4C>G	NP_001193784.1:n.102-4C>G