Canonical Allele Identifier: CA2684105767

Gene: TFR2

Linked Data

• gnomAD v4: 7-100620636-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100620636C>A , CM000669.2:g.100620636C>A	GRCh38
NC_000007.13:g.100218259C>A , CM000669.1:g.100218259C>A	GRCh37
NC_000007.12:g.100056195C>A	NCBI36
NG_007989.1:g.25915G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.*221G>T MANE Select	ENSP00000223051.3:n.*221G>T
ENST00000223051.7:c.*221G>T	ENSP00000223051.3:n.*221G>T
ENST00000431692.5:c.*1302G>T	ENSP00000413905.1:n.*1302G>T
ENST00000462090.5:n.1663G>T
ENST00000462107.1:c.*221G>T	ENSP00000420525.1:n.*221G>T
ENST00000465294.5:n.2547G>T
ENST00000476304.5:n.2248G>T
ENST00000490084.5:c.1980G>T
NM_001206855.1:c.*221G>T	NP_001193784.1:n.*221G>T
NM_003227.3:c.*221G>T	NP_003218.2:n.*221G>T
XM_005250553.3:c.*221G>T	XP_005250610.1:n.*221G>T
NM_001206855.2:c.*221G>T	NP_001193784.1:n.*221G>T
XM_005250553.4:c.*221G>T	XP_005250610.1:n.*221G>T
XM_017012573.1:c.*221G>T	XP_016868062.1:n.*221G>T
NM_003227.4:c.*221G>T MANE Select	NP_003218.2:n.*221G>T
NM_001206855.3:c.*221G>T	NP_001193784.1:n.*221G>T