Canonical Allele Identifier: CA507596
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs750829395
ExAC: 1:949378 G / T
gnomAD v2: 1-949378-G-T
gnomAD v4: 1-1013998-G-T
MyVariant Identifiers: chr1:g.949378G>T (hg19) chr1:g.1013998G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013998G>T , CM000663.2:g.1013998G>T GRCh38
NC_000001.10:g.949378G>T , CM000663.1:g.949378G>T GRCh37
NC_000001.9:g.939241G>T NCBI36
NG_033033.1:g.5532G>T
NG_033033.2:g.17861G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-7G>T ENSP00000485643.1:n.-7G>T
ENST00000649529.1:c.18G>T MANE Select ENSP00000496832.1:p.Thr6=
ENST00000379389.4:c.18G>T ENSP00000368699.4:p.Thr6=
ENST00000624652.1:c.-7G>T ENSP00000485313.1:n.-7G>T
ENST00000624697.3:c.-7G>T ENSP00000485643.1:n.-7G>T
NM_005101.3:c.18G>T NP_005092.1:p.Thr6=
NM_005101.4:c.18G>T MANE Select NP_005092.1:p.Thr6=
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