Canonical Allele Identifier: CA507679
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs760983415
ExAC: 1:949674 C / A
gnomAD v2: 1-949674-C-A
gnomAD v4: 1-1014294-C-A
MyVariant Identifiers: chr1:g.949674C>A (hg19) chr1:g.1014294C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014294C>A , CM000663.2:g.1014294C>A GRCh38
NC_000001.10:g.949674C>A , CM000663.1:g.949674C>A GRCh37
NC_000001.9:g.939537C>A NCBI36
NG_033033.1:g.5828C>A
NG_033033.2:g.18157C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.290C>A ENSP00000485643.1:p.Ala97Asp
ENST00000649529.1:c.314C>A MANE Select ENSP00000496832.1:p.Ala105Asp
ENST00000379389.4:c.314C>A ENSP00000368699.4:p.Ala105Asp
ENST00000624652.1:c.290C>A ENSP00000485313.1:p.Ala97Asp
ENST00000624697.3:c.290C>A ENSP00000485643.1:p.Ala97Asp
NM_005101.3:c.314C>A NP_005092.1:p.Ala105Asp
NM_005101.4:c.314C>A MANE Select NP_005092.1:p.Ala105Asp
Search 100 bp 5'
Search 100 bp 3'