Canonical Allele Identifier: CA830497684

Gene: TFR2

Linked Data

• ClinVar Variation Id: 908972
• ClinVar RCV Id: RCV001159773
• dbSNP Id: rs1314233014
• gnomAD v2: 7-100218200-T-G
• gnomAD v4: 7-100620577-T-G
• MyVariant Identifiers: chr7:g.100218200T>G (hg19) ; chr7:g.100620577T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100620577T>G , CM000669.2:g.100620577T>G	GRCh38
NC_000007.13:g.100218200T>G , CM000669.1:g.100218200T>G	GRCh37
NC_000007.12:g.100056136T>G	NCBI36
NG_007989.1:g.25974A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223051.8:c.*280A>C MANE Select	ENSP00000223051.3:n.*280A>C
ENST00000223051.7:c.*280A>C	ENSP00000223051.3:n.*280A>C
ENST00000431692.5:c.*1361A>C	ENSP00000413905.1:n.*1361A>C
ENST00000462090.5:n.1722A>C
ENST00000462107.1:c.*280A>C	ENSP00000420525.1:n.*280A>C
ENST00000465294.5:n.2606A>C
ENST00000476304.5:n.2307A>C
ENST00000490084.5:c.2039A>C
NM_001206855.1:c.*280A>C	NP_001193784.1:n.*280A>C
NM_003227.3:c.*280A>C	NP_003218.2:n.*280A>C
XM_005250553.3:c.*280A>C	XP_005250610.1:n.*280A>C
NM_001206855.2:c.*280A>C	NP_001193784.1:n.*280A>C
XM_005250553.4:c.*280A>C	XP_005250610.1:n.*280A>C
XM_017012573.1:c.*280A>C	XP_016868062.1:n.*280A>C
NM_003227.4:c.*280A>C MANE Select	NP_003218.2:n.*280A>C
NM_001206855.3:c.*280A>C	NP_001193784.1:n.*280A>C