Canonical Allele Identifier: CA415756003
Gene: ISG15 HGNC NCBI

Linked Data

ClinVar Variation Id: 1136240
ClinVar RCV Id: RCV001471805
dbSNP Id: rs2100541798
MyVariant Identifiers: chr1:g.949366C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013986C>T , CM000663.2:g.1013986C>T GRCh38
NC_000001.10:g.949366C>T , CM000663.1:g.949366C>T GRCh37
NC_000001.9:g.939229C>T NCBI36
NG_033033.1:g.5520C>T
NG_033033.2:g.17849C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-19C>T ENSP00000485643.1:n.-19C>T
ENST00000649529.1:c.6C>T MANE Select ENSP00000496832.1:p.Gly2=
ENST00000379389.4:c.6C>T ENSP00000368699.4:p.Gly2=
ENST00000624652.1:c.-19C>T ENSP00000485313.1:n.-19C>T
ENST00000624697.3:c.-19C>T ENSP00000485643.1:n.-19C>T
NM_005101.3:c.6C>T NP_005092.1:p.Gly2=
NM_005101.4:c.6C>T MANE Select NP_005092.1:p.Gly2=
Search 100 bp 5'
Search 100 bp 3'