Canonical Allele Identifier: CA368535020

Gene: TFR2

Linked Data

• gnomAD v4: 7-100633530-G-A
• MyVariant Identifiers: chr7:g.100231153G>A (hg19) ; chr7:g.100633530G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633530G>A , CM000669.2:g.100633530G>A	GRCh38
NC_000007.13:g.100231153G>A , CM000669.1:g.100231153G>A	GRCh37
NC_000007.12:g.100069089G>A	NCBI36
NG_007989.1:g.13021C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.500C>T MANE Select	ENSP00000223051.3:p.Ala167Val
ENST00000223051.7:c.500C>T	ENSP00000223051.3:p.Ala167Val
ENST00000431692.5:c.500C>T	ENSP00000413905.1:p.Ala167Val
ENST00000462107.1:c.500C>T	ENSP00000420525.1:p.Ala167Val
ENST00000465294.5:n.505C>T
ENST00000475011.1:n.29C>T
ENST00000476304.5:n.121C>T
NM_001206855.1:c.-14C>T	NP_001193784.1:n.-14C>T
NM_003227.3:c.500C>T	NP_003218.2:p.Ala167Val
XM_005250553.3:c.500C>T	XP_005250610.1:p.Ala167Val
XM_005250554.3:c.500C>T	XP_005250611.1:p.Ala167Val
NM_001206855.2:c.-14C>T	NP_001193784.1:n.-14C>T
XM_005250553.4:c.500C>T	XP_005250610.1:p.Ala167Val
XM_017012573.1:c.500C>T	XP_016868062.1:p.Ala167Val
NM_003227.4:c.500C>T MANE Select	NP_003218.2:p.Ala167Val
NM_001206855.3:c.-14C>T	NP_001193784.1:n.-14C>T