Canonical Allele Identifier: CA368521989

Gene: TFR2

Linked Data

• MyVariant Identifiers: chr7:g.100218669G>C (hg19) ; chr7:g.100621046G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100621046G>C , CM000669.2:g.100621046G>C	GRCh38
NC_000007.13:g.100218669G>C , CM000669.1:g.100218669G>C	GRCh37
NC_000007.12:g.100056605G>C	NCBI36
NG_007989.1:g.25505C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000223051.8:c.2217C>G MANE Select	ENSP00000223051.3:p.His739Gln
ENST00000223051.7:c.2217C>G	ENSP00000223051.3:p.His739Gln
ENST00000431692.5:c.*892C>G	ENSP00000413905.1:n.*892C>G
ENST00000462090.5:n.1253C>G
ENST00000462107.1:c.2217C>G	ENSP00000420525.1:p.His739Gln
ENST00000465294.5:n.2137C>G
ENST00000476304.5:n.1838C>G
ENST00000490084.5:c.1570C>G
NM_001206855.1:c.1704C>G	NP_001193784.1:p.His568Gln
NM_003227.3:c.2217C>G	NP_003218.2:p.His739Gln
XM_005250553.3:c.2217C>G	XP_005250610.1:p.His739Gln
NM_001206855.2:c.1704C>G	NP_001193784.1:p.His568Gln
XM_005250553.4:c.2217C>G	XP_005250610.1:p.His739Gln
XM_017012573.1:c.2217C>G	XP_016868062.1:p.His739Gln
NM_003227.4:c.2217C>G MANE Select	NP_003218.2:p.His739Gln
NM_001206855.3:c.1704C>G	NP_001193784.1:p.His568Gln