Canonical Allele Identifier: CA507633
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs373479211
ExAC: 1:949510 C / G
gnomAD v2: 1-949510-C-G
gnomAD v4: 1-1014130-C-G
MyVariant Identifiers: chr1:g.949510C>G (hg19) chr1:g.1014130C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014130C>G , CM000663.2:g.1014130C>G GRCh38
NC_000001.10:g.949510C>G , CM000663.1:g.949510C>G GRCh37
NC_000001.9:g.939373C>G NCBI36
NG_033033.1:g.5664C>G
NG_033033.2:g.17993C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.126C>G ENSP00000485643.1:p.Ser42Arg
ENST00000649529.1:c.150C>G MANE Select ENSP00000496832.1:p.Ser50Arg
ENST00000379389.4:c.150C>G ENSP00000368699.4:p.Ser50Arg
ENST00000624652.1:c.126C>G ENSP00000485313.1:p.Ser42Arg
ENST00000624697.3:c.126C>G ENSP00000485643.1:p.Ser42Arg
NM_005101.3:c.150C>G NP_005092.1:p.Ser50Arg
NM_005101.4:c.150C>G MANE Select NP_005092.1:p.Ser50Arg
Search 100 bp 5'
Search 100 bp 3'