Canonical Allele Identifier: CA337804661
Gene: ISG15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.949617T>A (hg19) chr1:g.1014237T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014237T>A , CM000663.2:g.1014237T>A GRCh38
NC_000001.10:g.949617T>A , CM000663.1:g.949617T>A GRCh37
NC_000001.9:g.939480T>A NCBI36
NG_033033.1:g.5771T>A
NG_033033.2:g.18100T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.233T>A ENSP00000485643.1:p.Val78Glu
ENST00000649529.1:c.257T>A MANE Select ENSP00000496832.1:p.Val86Glu
ENST00000379389.4:c.257T>A ENSP00000368699.4:p.Val86Glu
ENST00000624652.1:c.233T>A ENSP00000485313.1:p.Val78Glu
ENST00000624697.3:c.233T>A ENSP00000485643.1:p.Val78Glu
NM_005101.3:c.257T>A NP_005092.1:p.Val86Glu
NM_005101.4:c.257T>A MANE Select NP_005092.1:p.Val86Glu
Search 100 bp 5'
Search 100 bp 3'