Canonical Allele Identifier: CA507593
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs761477971
ExAC: 1:949376 A / G
gnomAD v2: 1-949376-A-G
gnomAD v4: 1-1013996-A-G
MyVariant Identifiers: chr1:g.949376A>G (hg19) chr1:g.1013996A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013996A>G , CM000663.2:g.1013996A>G GRCh38
NC_000001.10:g.949376A>G , CM000663.1:g.949376A>G GRCh37
NC_000001.9:g.939239A>G NCBI36
NG_033033.1:g.5530A>G
NG_033033.2:g.17859A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-9A>G ENSP00000485643.1:n.-9A>G
ENST00000649529.1:c.16A>G MANE Select ENSP00000496832.1:p.Thr6Ala
ENST00000379389.4:c.16A>G ENSP00000368699.4:p.Thr6Ala
ENST00000624652.1:c.-9A>G ENSP00000485313.1:n.-9A>G
ENST00000624697.3:c.-9A>G ENSP00000485643.1:n.-9A>G
NM_005101.3:c.16A>G NP_005092.1:p.Thr6Ala
NM_005101.4:c.16A>G MANE Select NP_005092.1:p.Thr6Ala
Search 100 bp 5'
Search 100 bp 3'