Canonical Allele Identifier: CA368523011

Gene: TFR2

Linked Data

• dbSNP Id: rs1348067198
• gnomAD v2: 7-100224503-C-G
• gnomAD v4: 7-100626880-C-G
• MyVariant Identifiers: chr7:g.100224503C>G (hg19) ; chr7:g.100626880C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100626880C>G , CM000669.2:g.100626880C>G	GRCh38
NC_000007.13:g.100224503C>G , CM000669.1:g.100224503C>G	GRCh37
NC_000007.12:g.100062439C>G	NCBI36
NG_007989.1:g.19671G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.2019G>C MANE Select	ENSP00000223051.3:p.Trp673Cys
ENST00000223051.7:c.2019G>C	ENSP00000223051.3:p.Trp673Cys
ENST00000431692.5:c.*694G>C	ENSP00000413905.1:n.*694G>C
ENST00000461176.1:n.365G>C
ENST00000462090.5:n.1055G>C
ENST00000462107.1:c.2019G>C	ENSP00000420525.1:p.Trp673Cys
ENST00000465294.5:n.1939G>C
ENST00000476304.5:n.1640G>C
ENST00000490084.5:c.1372G>C
NM_001206855.1:c.1506G>C	NP_001193784.1:p.Trp502Cys
NM_003227.3:c.2019G>C	NP_003218.2:p.Trp673Cys
XM_005250553.3:c.2019G>C	XP_005250610.1:p.Trp673Cys
XM_005250554.3:c.2019G>C	XP_005250611.1:p.Trp673Cys
XR_927814.1:n.434-4276C>G
NM_001206855.2:c.1506G>C	NP_001193784.1:p.Trp502Cys
XM_005250553.4:c.2019G>C	XP_005250610.1:p.Trp673Cys
XM_017012573.1:c.2019G>C	XP_016868062.1:p.Trp673Cys
NM_003227.4:c.2019G>C MANE Select	NP_003218.2:p.Trp673Cys
NM_001206855.3:c.1506G>C	NP_001193784.1:p.Trp502Cys