Canonical Allele Identifier: CA368535026

Gene: TFR2

Linked Data

• dbSNP Id: rs1803511674
• gnomAD v4: 7-100633531-C-T
• MyVariant Identifiers: chr7:g.100231154C>T (hg19) ; chr7:g.100633531C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633531C>T , CM000669.2:g.100633531C>T	GRCh38
NC_000007.13:g.100231154C>T , CM000669.1:g.100231154C>T	GRCh37
NC_000007.12:g.100069090C>T	NCBI36
NG_007989.1:g.13020G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.499G>A MANE Select	ENSP00000223051.3:p.Ala167Thr
ENST00000223051.7:c.499G>A	ENSP00000223051.3:p.Ala167Thr
ENST00000431692.5:c.499G>A	ENSP00000413905.1:p.Ala167Thr
ENST00000462107.1:c.499G>A	ENSP00000420525.1:p.Ala167Thr
ENST00000465294.5:n.504G>A
ENST00000475011.1:n.28G>A
ENST00000476304.5:n.120G>A
NM_001206855.1:c.-15G>A	NP_001193784.1:n.-15G>A
NM_003227.3:c.499G>A	NP_003218.2:p.Ala167Thr
XM_005250553.3:c.499G>A	XP_005250610.1:p.Ala167Thr
XM_005250554.3:c.499G>A	XP_005250611.1:p.Ala167Thr
NM_001206855.2:c.-15G>A	NP_001193784.1:n.-15G>A
XM_005250553.4:c.499G>A	XP_005250610.1:p.Ala167Thr
XM_017012573.1:c.499G>A	XP_016868062.1:p.Ala167Thr
NM_003227.4:c.499G>A MANE Select	NP_003218.2:p.Ala167Thr
NM_001206855.3:c.-15G>A	NP_001193784.1:n.-15G>A