Canonical Allele Identifier: CA337803839
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949482T>C (hg19) chr1:g.1014102T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014102T>C , CM000663.2:g.1014102T>C GRCh38
NC_000001.10:g.949482T>C , CM000663.1:g.949482T>C GRCh37
NC_000001.9:g.939345T>C NCBI36
NG_033033.1:g.5636T>C
NG_033033.2:g.17965T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.98T>C ENSP00000485643.1:p.Phe33Ser
ENST00000649529.1:c.122T>C MANE Select ENSP00000496832.1:p.Phe41Ser
ENST00000379389.4:c.122T>C ENSP00000368699.4:p.Phe41Ser
ENST00000624652.1:c.98T>C ENSP00000485313.1:p.Phe33Ser
ENST00000624697.3:c.98T>C ENSP00000485643.1:p.Phe33Ser
NM_005101.3:c.122T>C NP_005092.1:p.Phe41Ser
NM_005101.4:c.122T>C MANE Select NP_005092.1:p.Phe41Ser
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