Canonical Allele Identifier: CA368533583
Gene: TFR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.100633013G>T , CM000669.2:g.100633013G>T GRCh38
NC_000007.13:g.100230636G>T , CM000669.1:g.100230636G>T GRCh37
NC_000007.12:g.100068572G>T NCBI36
NG_007989.1:g.13538C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000223051.8:c.837C>A MANE Select ENSP00000223051.3:p.Ser279Arg
ENST00000223051.7:c.837C>A ENSP00000223051.3:p.Ser279Arg
ENST00000431692.5:c.837C>A ENSP00000413905.1:p.Ser279Arg
ENST00000462090.5:n.78C>A
ENST00000462107.1:c.837C>A ENSP00000420525.1:p.Ser279Arg
ENST00000465294.5:n.842C>A
ENST00000473374.5:n.287C>A
ENST00000473571.1:n.291C>A
ENST00000475011.1:n.366C>A
ENST00000476304.5:n.458C>A
ENST00000490084.5:c.92C>A
NM_001206855.1:c.324C>A NP_001193784.1:p.Ser108Arg
NM_003227.3:c.837C>A NP_003218.2:p.Ser279Arg
XM_005250553.3:c.837C>A XP_005250610.1:p.Ser279Arg
XM_005250554.3:c.837C>A XP_005250611.1:p.Ser279Arg
NM_001206855.2:c.324C>A NP_001193784.1:p.Ser108Arg
XM_005250553.4:c.837C>A XP_005250610.1:p.Ser279Arg
XM_017012573.1:c.837C>A XP_016868062.1:p.Ser279Arg
NM_003227.4:c.837C>A MANE Select NP_003218.2:p.Ser279Arg
NM_001206855.3:c.324C>A NP_001193784.1:p.Ser108Arg