Canonical Allele Identifier: CA14885445
Gene: IFNAR1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1012335

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.33341701G>C , CM000683.2:g.33341701G>C GRCh38
NC_000021.8:g.34714007G>C , CM000683.1:g.34714007G>C GRCh37
NC_000021.7:g.33635877G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_000629.2:c.376+527G>C VV NP_000620.2:p.=
XM_005260964.1:c.169+527G>C XP_005261021.1:p.=
XM_011529552.1:c.376+527G>C XP_011527854.1:p.=
XM_005260964.2:c.169+527G>C
XM_011529552.2:c.376+527G>C
ENST00000270139.7:c.376+527G>C ENSP00000270139.3:p.=
ENST00000442071.1:c.376+527G>C ENSP00000400161.1:p.=