Canonical Allele Identifier: CA368524888

Gene: TFR2

Linked Data

• gnomAD v4: 7-100627375-C-G
• MyVariant Identifiers: chr7:g.100224998C>G (hg19) ; chr7:g.100627375C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100627375C>G , CM000669.2:g.100627375C>G	GRCh38
NC_000007.13:g.100224998C>G , CM000669.1:g.100224998C>G	GRCh37
NC_000007.12:g.100062934C>G	NCBI36
NG_007989.1:g.19176G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.1884G>C MANE Select	ENSP00000223051.3:p.Gln628His
ENST00000223051.7:c.1884G>C	ENSP00000223051.3:p.Gln628His
ENST00000431692.5:c.*559G>C	ENSP00000413905.1:n.*559G>C
ENST00000461176.1:n.230G>C
ENST00000462090.5:n.920G>C
ENST00000462107.1:c.1884G>C	ENSP00000420525.1:p.Gln628His
ENST00000465294.5:n.1804G>C
ENST00000476304.5:n.1505G>C
ENST00000490084.5:c.1237G>C
NM_001206855.1:c.1371G>C	NP_001193784.1:p.Gln457His
NM_003227.3:c.1884G>C	NP_003218.2:p.Gln628His
XM_005250553.3:c.1884G>C	XP_005250610.1:p.Gln628His
XM_005250554.3:c.1884G>C	XP_005250611.1:p.Gln628His
XR_927814.1:n.434-3781C>G
NM_001206855.2:c.1371G>C	NP_001193784.1:p.Gln457His
XM_005250553.4:c.1884G>C	XP_005250610.1:p.Gln628His
XM_017012573.1:c.1884G>C	XP_016868062.1:p.Gln628His
NM_003227.4:c.1884G>C MANE Select	NP_003218.2:p.Gln628His
NM_001206855.3:c.1371G>C	NP_001193784.1:p.Gln457His