Canonical Allele Identifier: CA2386632777

Gene: IFNAR1

Linked Data

• dbSNP Id: rs2083292947

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.33341611C>T , CM000683.2:g.33341611C>T	GRCh38
NC_000021.8:g.34713917C>T , CM000683.1:g.34713917C>T	GRCh37
NC_000021.7:g.33635787C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000442071.3:c.376+437C>T	ENSP00000400161.3:n.376+437C>T
ENST00000651609.2:c.*93+437C>T	ENSP00000498594.1:n.*93+437C>T
ENST00000652450.2:c.169+437C>T	ENSP00000498654.1:n.169+437C>T
ENST00000652513.2:c.376+437C>T	ENSP00000498491.1:n.376+437C>T
ENST00000652654.3:c.376+437C>T	ENSP00000498666.1:n.376+437C>T
ENST00000700045.1:n.503+437C>T
ENST00000700046.1:c.201-1657C>T	ENSP00000514762.1:n.201-1657C>T
ENST00000700080.1:c.169+437C>T	ENSP00000514785.1:n.169+437C>T
ENST00000700084.1:c.-89-3635C>T	ENSP00000514786.1:n.-89-3635C>T
ENST00000700087.1:n.497+437C>T
ENST00000700099.1:n.894C>T
ENST00000700301.1:n.497+437C>T
ENST00000703514.1:c.376+437C>T	ENSP00000515347.1:n.376+437C>T
ENST00000703515.1:c.376+437C>T	ENSP00000515348.1:n.376+437C>T
ENST00000703516.1:c.201-3635C>T	ENSP00000515349.1:n.201-3635C>T
ENST00000703556.1:c.376+437C>T	ENSP00000515372.1:n.376+437C>T
ENST00000703557.1:c.376+437C>T	ENSP00000515373.1:n.376+437C>T
ENST00000703561.1:c.376+437C>T	ENSP00000515377.1:n.376+437C>T
ENST00000703562.1:c.376+437C>T	ENSP00000515378.1:n.376+437C>T
ENST00000703563.1:c.376+437C>T	ENSP00000515379.1:n.376+437C>T
ENST00000703564.1:c.*93+437C>T	ENSP00000515380.1:n.*93+437C>T
ENST00000703565.1:c.376+437C>T	ENSP00000515381.1:n.376+437C>T
ENST00000703778.1:n.422+437C>T
ENST00000703779.1:c.201-1657C>T	ENSP00000515477.1:n.201-1657C>T
ENST00000270139.8:c.376+437C>T MANE Select	ENSP00000270139.3:n.376+437C>T
ENST00000442071.2:c.376+437C>T	ENSP00000400161.2:n.376+437C>T
ENST00000651609.1:c.*93+437C>T	ENSP00000498594.1:n.*93+437C>T
ENST00000652450.1:c.169+437C>T	ENSP00000498654.1:n.169+437C>T
ENST00000652513.1:c.376+437C>T	ENSP00000498491.1:n.376+437C>T
ENST00000652601.1:c.376+437C>T	ENSP00000498231.1:n.376+437C>T
ENST00000652654.1:c.376+437C>T	ENSP00000498666.1:n.376+437C>T
ENST00000270139.7:c.376+437C>T	ENSP00000270139.3:n.376+437C>T
ENST00000442071.1:c.376+437C>T	ENSP00000400161.1:n.376+437C>T
NM_000629.2:c.376+437C>T	NP_000620.2:n.376+437C>T
XM_005260964.1:c.169+437C>T	XP_005261021.1:n.169+437C>T
XM_011529552.1:c.376+437C>T	XP_011527854.1:n.376+437C>T
XM_005260964.2:c.169+437C>T	XP_005261021.1:n.169+437C>T
XM_011529552.2:c.376+437C>T	XP_011527854.1:n.376+437C>T
NM_000629.3:c.376+437C>T MANE Select	NP_000620.2:n.376+437C>T
NM_001384498.1:c.376+437C>T	NP_001371427.1:n.376+437C>T
NM_001384499.1:c.376+437C>T	NP_001371428.1:n.376+437C>T
NM_001384500.1:c.-411+437C>T	NP_001371429.1:n.-411+437C>T
NM_001384501.1:c.376+437C>T	NP_001371430.1:n.376+437C>T
NM_001384502.1:c.-87+437C>T	NP_001371431.1:n.-87+437C>T
NM_001384503.1:c.376+437C>T	NP_001371432.1:n.376+437C>T
NM_001384504.1:c.169+437C>T	NP_001371433.1:n.169+437C>T