Canonical Allele Identifier: CA415756983
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949619A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014239A>C , CM000663.2:g.1014239A>C GRCh38
NC_000001.10:g.949619A>C , CM000663.1:g.949619A>C GRCh37
NC_000001.9:g.939482A>C NCBI36
NG_033033.1:g.5773A>C
NG_033033.2:g.18102A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.235A>C ENSP00000485643.1:p.Arg79=
ENST00000649529.1:c.259A>C MANE Select ENSP00000496832.1:p.Arg87=
ENST00000379389.4:c.259A>C ENSP00000368699.4:p.Arg87=
ENST00000624652.1:c.235A>C ENSP00000485313.1:p.Arg79=
ENST00000624697.3:c.235A>C ENSP00000485643.1:p.Arg79=
NM_005101.3:c.259A>C NP_005092.1:p.Arg87=
NM_005101.4:c.259A>C MANE Select NP_005092.1:p.Arg87=
Search 100 bp 5'
Search 100 bp 3'