Canonical Allele Identifier: CA368534077

Gene: TFR2

Linked Data

• dbSNP Id: rs1305811255
• gnomAD v4: 7-100633099-C-T
• MyVariant Identifiers: chr7:g.100230722C>T (hg19) ; chr7:g.100633099C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633099C>T , CM000669.2:g.100633099C>T	GRCh38
NC_000007.13:g.100230722C>T , CM000669.1:g.100230722C>T	GRCh37
NC_000007.12:g.100068658C>T	NCBI36
NG_007989.1:g.13452G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.751G>A MANE Select	ENSP00000223051.3:p.Gly251Arg
ENST00000223051.7:c.751G>A	ENSP00000223051.3:p.Gly251Arg
ENST00000431692.5:c.751G>A	ENSP00000413905.1:p.Gly251Arg
ENST00000462107.1:c.751G>A	ENSP00000420525.1:p.Gly251Arg
ENST00000465294.5:n.756G>A
ENST00000473374.5:n.201G>A
ENST00000473571.1:n.205G>A
ENST00000475011.1:n.280G>A
ENST00000476304.5:n.372G>A
ENST00000490084.5:c.6G>A
NM_001206855.1:c.238G>A	NP_001193784.1:p.Gly80Arg
NM_003227.3:c.751G>A	NP_003218.2:p.Gly251Arg
XM_005250553.3:c.751G>A	XP_005250610.1:p.Gly251Arg
XM_005250554.3:c.751G>A	XP_005250611.1:p.Gly251Arg
NM_001206855.2:c.238G>A	NP_001193784.1:p.Gly80Arg
XM_005250553.4:c.751G>A	XP_005250610.1:p.Gly251Arg
XM_017012573.1:c.751G>A	XP_016868062.1:p.Gly251Arg
NM_003227.4:c.751G>A MANE Select	NP_003218.2:p.Gly251Arg
NM_001206855.3:c.238G>A	NP_001193784.1:p.Gly80Arg