Canonical Allele Identifier: CA337804994
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949677A>C (hg19) chr1:g.1014297A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014297A>C , CM000663.2:g.1014297A>C GRCh38
NC_000001.10:g.949677A>C , CM000663.1:g.949677A>C GRCh37
NC_000001.9:g.939540A>C NCBI36
NG_033033.1:g.5831A>C
NG_033033.2:g.18160A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.293A>C ENSP00000485643.1:p.His98Pro
ENST00000649529.1:c.317A>C MANE Select ENSP00000496832.1:p.His106Pro
ENST00000379389.4:c.317A>C ENSP00000368699.4:p.His106Pro
ENST00000624652.1:c.293A>C ENSP00000485313.1:p.His98Pro
ENST00000624697.3:c.293A>C ENSP00000485643.1:p.His98Pro
NM_005101.3:c.317A>C NP_005092.1:p.His106Pro
NM_005101.4:c.317A>C MANE Select NP_005092.1:p.His106Pro
Search 100 bp 5'
Search 100 bp 3'