Canonical Allele Identifier: CA2715377554

Gene: TFR2

Linked Data

• dbSNP Id: rs1803077305

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100620712C>T , CM000669.2:g.100620712C>T	GRCh38
NC_000007.13:g.100218335C>T , CM000669.1:g.100218335C>T	GRCh37
NC_000007.12:g.100056271C>T	NCBI36
NG_007989.1:g.25839G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.*145G>A MANE Select	ENSP00000223051.3:n.*145G>A
ENST00000223051.7:c.*145G>A	ENSP00000223051.3:n.*145G>A
ENST00000431692.5:c.*1226G>A	ENSP00000413905.1:n.*1226G>A
ENST00000462090.5:n.1587G>A
ENST00000462107.1:c.*145G>A	ENSP00000420525.1:n.*145G>A
ENST00000465294.5:n.2471G>A
ENST00000476304.5:n.2172G>A
ENST00000490084.5:c.1904G>A
NM_001206855.1:c.*145G>A	NP_001193784.1:n.*145G>A
NM_003227.3:c.*145G>A	NP_003218.2:n.*145G>A
XM_005250553.3:c.*145G>A	XP_005250610.1:n.*145G>A
NM_001206855.2:c.*145G>A	NP_001193784.1:n.*145G>A
XM_005250553.4:c.*145G>A	XP_005250610.1:n.*145G>A
XM_017012573.1:c.*145G>A	XP_016868062.1:n.*145G>A
NM_003227.4:c.*145G>A MANE Select	NP_003218.2:n.*145G>A
NM_001206855.3:c.*145G>A	NP_001193784.1:n.*145G>A