Canonical Allele Identifier: CA507623
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs779734087
ExAC: 1:949490 C / G
gnomAD v2: 1-949490-C-G
gnomAD v4: 1-1014110-C-G
MyVariant Identifiers: chr1:g.949490C>G (hg19) chr1:g.1014110C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014110C>G , CM000663.2:g.1014110C>G GRCh38
NC_000001.10:g.949490C>G , CM000663.1:g.949490C>G GRCh37
NC_000001.9:g.939353C>G NCBI36
NG_033033.1:g.5644C>G
NG_033033.2:g.17973C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.106C>G ENSP00000485643.1:p.Arg36Gly
ENST00000649529.1:c.130C>G MANE Select ENSP00000496832.1:p.Arg44Gly
ENST00000379389.4:c.130C>G ENSP00000368699.4:p.Arg44Gly
ENST00000624652.1:c.106C>G ENSP00000485313.1:p.Arg36Gly
ENST00000624697.3:c.106C>G ENSP00000485643.1:p.Arg36Gly
NM_005101.3:c.130C>G NP_005092.1:p.Arg44Gly
NM_005101.4:c.130C>G MANE Select NP_005092.1:p.Arg44Gly
Search 100 bp 5'
Search 100 bp 3'