Canonical Allele Identifier: CA2176711128

Gene: TNFAIP8L3 PIRC66 MIR4713HG

Linked Data

• dbSNP Id: rs2065406850

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51083570A>C , CM000677.2:g.51083570A>C	GRCh38
NC_000015.9:g.51375767A>C , CM000677.1:g.51375767A>C	GRCh37
NC_000015.8:g.49163059A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000637513.2:c.52+10974T>G (TNFAIP8L3) MANE Select	ENSP00000489743.1:n.52+10974T>G
ENST00000649177.1:c.-87+10841T>G (TNFAIP8L3)	ENSP00000498365.1:n.-87+10841T>G
ENST00000327536.5:c.316+10974T>G (TNFAIP8L3)	ENSP00000328016.5:n.316+10974T>G
NM_001311175.1:c.52+10974T>G (TNFAIP8L3)	NP_001298104.1:n.52+10974T>G
NM_207381.3:c.316+10974T>G (TNFAIP8L3)	NP_997264.2:n.316+10974T>G
XM_006720500.2:c.-87+1477T>G (TNFAIP8L3)	XP_006720563.1:n.-87+1477T>G
XR_932222.1:n.98+45889A>C (PIRC66)
NR_146310.1:n.194+45889A>C (MIR4713HG)
XM_017022169.1:c.-87+1477T>G (TNFAIP8L3)	XP_016877658.1:n.-87+1477T>G
NM_001311175.2:c.52+10974T>G (TNFAIP8L3) MANE Select	NP_001298104.1:n.52+10974T>G
NM_207381.4:c.316+10974T>G (TNFAIP8L3)	NP_997264.2:n.316+10974T>G