Canonical Allele Identifier: CA16724837
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs903332079
gnomAD v3: 1-1013861-T-C
gnomAD v4: 1-1013861-T-C
MyVariant Identifiers: chr1:g.949241T>C (hg19) chr1:g.1013861T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013861T>C , CM000663.2:g.1013861T>C GRCh38
NC_000001.10:g.949241T>C , CM000663.1:g.949241T>C GRCh37
NC_000001.9:g.939104T>C NCBI36
NG_033033.1:g.5395T>C
NG_033033.2:g.17724T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-123T>C ENSP00000485643.1:n.-21-123T>C
ENST00000649529.1:c.4-123T>C MANE Select ENSP00000496832.1:n.4-123T>C
ENST00000379389.4:c.4-123T>C ENSP00000368699.4:n.4-123T>C
ENST00000624652.1:c.-21-123T>C ENSP00000485313.1:n.-21-123T>C
ENST00000624697.3:c.-21-123T>C ENSP00000485643.1:n.-21-123T>C
NM_005101.3:c.4-123T>C NP_005092.1:n.4-123T>C
NM_005101.4:c.4-123T>C MANE Select NP_005092.1:n.4-123T>C
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