Canonical Allele Identifier: CA337804490
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949592T>A (hg19) chr1:g.1014212T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014212T>A , CM000663.2:g.1014212T>A GRCh38
NC_000001.10:g.949592T>A , CM000663.1:g.949592T>A GRCh37
NC_000001.9:g.939455T>A NCBI36
NG_033033.1:g.5746T>A
NG_033033.2:g.18075T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.208T>A ENSP00000485643.1:p.Cys70Ser
ENST00000649529.1:c.232T>A MANE Select ENSP00000496832.1:p.Cys78Ser
ENST00000379389.4:c.232T>A ENSP00000368699.4:p.Cys78Ser
ENST00000624652.1:c.208T>A ENSP00000485313.1:p.Cys70Ser
ENST00000624697.3:c.208T>A ENSP00000485643.1:p.Cys70Ser
NM_005101.3:c.232T>A NP_005092.1:p.Cys78Ser
NM_005101.4:c.232T>A MANE Select NP_005092.1:p.Cys78Ser
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