Canonical Allele Identifier: CA507616
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs1126625
ExAC: 1:949468 C / A
gnomAD v2: 1-949468-C-A
gnomAD v4: 1-1014088-C-A
MyVariant Identifiers: chr1:g.949468C>A (hg19) chr1:g.1014088C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014088C>A , CM000663.2:g.1014088C>A GRCh38
NC_000001.10:g.949468C>A , CM000663.1:g.949468C>A GRCh37
NC_000001.9:g.939331C>A NCBI36
NG_033033.1:g.5622C>A
NG_033033.2:g.17951C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.84C>A ENSP00000485643.1:p.Ile28=
ENST00000649529.1:c.108C>A MANE Select ENSP00000496832.1:p.Ile36=
ENST00000379389.4:c.108C>A ENSP00000368699.4:p.Ile36=
ENST00000624652.1:c.84C>A ENSP00000485313.1:p.Ile28=
ENST00000624697.3:c.84C>A ENSP00000485643.1:p.Ile28=
NM_005101.3:c.108C>A NP_005092.1:p.Ile36=
NM_005101.4:c.108C>A MANE Select NP_005092.1:p.Ile36=
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