Canonical Allele Identifier: CA337803998
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949509G>C (hg19) chr1:g.1014129G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014129G>C , CM000663.2:g.1014129G>C GRCh38
NC_000001.10:g.949509G>C , CM000663.1:g.949509G>C GRCh37
NC_000001.9:g.939372G>C NCBI36
NG_033033.1:g.5663G>C
NG_033033.2:g.17992G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.125G>C ENSP00000485643.1:p.Ser42Thr
ENST00000649529.1:c.149G>C MANE Select ENSP00000496832.1:p.Ser50Thr
ENST00000379389.4:c.149G>C ENSP00000368699.4:p.Ser50Thr
ENST00000624652.1:c.125G>C ENSP00000485313.1:p.Ser42Thr
ENST00000624697.3:c.125G>C ENSP00000485643.1:p.Ser42Thr
NM_005101.3:c.149G>C NP_005092.1:p.Ser50Thr
NM_005101.4:c.149G>C MANE Select NP_005092.1:p.Ser50Thr
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