Canonical Allele Identifier: CA456750200

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100230729G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100633106G>C , CM000669.2:g.100633106G>C	GRCh38
NC_000007.13:g.100230729G>C , CM000669.1:g.100230729G>C	GRCh37
NC_000007.12:g.100068665G>C	NCBI36
NG_007989.1:g.13445C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000223051.8:c.744C>G MANE Select	ENSP00000223051.3:p.Ala248=
ENST00000223051.7:c.744C>G	ENSP00000223051.3:p.Ala248=
ENST00000431692.5:c.744C>G	ENSP00000413905.1:p.Ala248=
ENST00000462107.1:c.744C>G	ENSP00000420525.1:p.Ala248=
ENST00000465294.5:n.749C>G
ENST00000473374.5:n.194C>G
ENST00000473571.1:n.198C>G
ENST00000475011.1:n.273C>G
ENST00000476304.5:n.365C>G
NM_001206855.1:c.231C>G	NP_001193784.1:p.Ala77=
NM_003227.3:c.744C>G	NP_003218.2:p.Ala248=
XM_005250553.3:c.744C>G	XP_005250610.1:p.Ala248=
XM_005250554.3:c.744C>G	XP_005250611.1:p.Ala248=
NM_001206855.2:c.231C>G	NP_001193784.1:p.Ala77=
XM_005250553.4:c.744C>G	XP_005250610.1:p.Ala248=
XM_017012573.1:c.744C>G	XP_016868062.1:p.Ala248=
NM_003227.4:c.744C>G MANE Select	NP_003218.2:p.Ala248=
NM_001206855.3:c.231C>G	NP_001193784.1:p.Ala77=