Canonical Allele Identifier: CA415756900
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1014220-A-G
MyVariant Identifiers: chr1:g.949600A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014220A>G , CM000663.2:g.1014220A>G GRCh38
NC_000001.10:g.949600A>G , CM000663.1:g.949600A>G GRCh37
NC_000001.9:g.939463A>G NCBI36
NG_033033.1:g.5754A>G
NG_033033.2:g.18083A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.216A>G ENSP00000485643.1:p.Glu72=
ENST00000649529.1:c.240A>G MANE Select ENSP00000496832.1:p.Glu80=
ENST00000379389.4:c.240A>G ENSP00000368699.4:p.Glu80=
ENST00000624652.1:c.216A>G ENSP00000485313.1:p.Glu72=
ENST00000624697.3:c.216A>G ENSP00000485643.1:p.Glu72=
NM_005101.3:c.240A>G NP_005092.1:p.Glu80=
NM_005101.4:c.240A>G MANE Select NP_005092.1:p.Glu80=
Search 100 bp 5'
Search 100 bp 3'