Canonical Allele Identifier: CA337804602
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949609C>A (hg19) chr1:g.1014229C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014229C>A , CM000663.2:g.1014229C>A GRCh38
NC_000001.10:g.949609C>A , CM000663.1:g.949609C>A GRCh37
NC_000001.9:g.939472C>A NCBI36
NG_033033.1:g.5763C>A
NG_033033.2:g.18092C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.225C>A ENSP00000485643.1:p.Ser75Arg
ENST00000649529.1:c.249C>A MANE Select ENSP00000496832.1:p.Ser83Arg
ENST00000379389.4:c.249C>A ENSP00000368699.4:p.Ser83Arg
ENST00000624652.1:c.225C>A ENSP00000485313.1:p.Ser75Arg
ENST00000624697.3:c.225C>A ENSP00000485643.1:p.Ser75Arg
NM_005101.3:c.249C>A NP_005092.1:p.Ser83Arg
NM_005101.4:c.249C>A MANE Select NP_005092.1:p.Ser83Arg
Search 100 bp 5'
Search 100 bp 3'