Canonical Allele Identifier: CA507599
Gene: ISG15 HGNC NCBI

Linked Data

ClinVar Variation Id: 1099068
ClinVar RCV Id: RCV001421259
dbSNP Id: rs369889443
ExAC: 1:949399 C / T
gnomAD v2: 1-949399-C-T
gnomAD v3: 1-1014019-C-T
gnomAD v4: 1-1014019-C-T
MyVariant Identifiers: chr1:g.949399C>T (hg19) chr1:g.1014019C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014019C>T , CM000663.2:g.1014019C>T GRCh38
NC_000001.10:g.949399C>T , CM000663.1:g.949399C>T GRCh37
NC_000001.9:g.939262C>T NCBI36
NG_033033.1:g.5553C>T
NG_033033.2:g.17882C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.15C>T ENSP00000485643.1:p.Asn5=
ENST00000649529.1:c.39C>T MANE Select ENSP00000496832.1:p.Asn13=
ENST00000379389.4:c.39C>T ENSP00000368699.4:p.Asn13=
ENST00000624652.1:c.15C>T ENSP00000485313.1:p.Asn5=
ENST00000624697.3:c.15C>T ENSP00000485643.1:p.Asn5=
NM_005101.3:c.39C>T NP_005092.1:p.Asn13=
NM_005101.4:c.39C>T MANE Select NP_005092.1:p.Asn13=
Search 100 bp 5'
Search 100 bp 3'