Canonical Allele Identifier: CA337804632
Gene: ISG15 HGNC NCBI

Linked Data

ClinVar Variation Id: 1396122
ClinVar RCV Id: RCV001902912
dbSNP Id: rs1644250077
MyVariant Identifiers: chr1:g.949616G>A (hg19) chr1:g.1014236G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014236G>A , CM000663.2:g.1014236G>A GRCh38
NC_000001.10:g.949616G>A , CM000663.1:g.949616G>A GRCh37
NC_000001.9:g.939479G>A NCBI36
NG_033033.1:g.5770G>A
NG_033033.2:g.18099G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.232G>A ENSP00000485643.1:p.Val78Met
ENST00000649529.1:c.256G>A MANE Select ENSP00000496832.1:p.Val86Met
ENST00000379389.4:c.256G>A ENSP00000368699.4:p.Val86Met
ENST00000624652.1:c.232G>A ENSP00000485313.1:p.Val78Met
ENST00000624697.3:c.232G>A ENSP00000485643.1:p.Val78Met
NM_005101.3:c.256G>A NP_005092.1:p.Val86Met
NM_005101.4:c.256G>A MANE Select NP_005092.1:p.Val86Met
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