Canonical Allele Identifier: CA15105791
Gene: ISG15 HGNC NCBI

Linked Data

ClinVar Variation Id: 1185395
ClinVar RCV Id: RCV001544206
dbSNP Id: rs2465124
gnomAD v2: 1-949235-G-A
gnomAD v3: 1-1013855-G-A
gnomAD v4: 1-1013855-G-A
MyVariant Identifiers: chr1:g.949235G>A (hg19) chr1:g.1013855G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013855G>A , CM000663.2:g.1013855G>A GRCh38
NC_000001.10:g.949235G>A , CM000663.1:g.949235G>A GRCh37
NC_000001.9:g.939098G>A NCBI36
NG_033033.1:g.5389G>A
NG_033033.2:g.17718G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-129G>A ENSP00000485643.1:n.-21-129G>A
ENST00000649529.1:c.4-129G>A MANE Select ENSP00000496832.1:n.4-129G>A
ENST00000379389.4:c.4-129G>A ENSP00000368699.4:n.4-129G>A
ENST00000624652.1:c.-21-129G>A ENSP00000485313.1:n.-21-129G>A
ENST00000624697.3:c.-21-129G>A ENSP00000485643.1:n.-21-129G>A
NM_005101.3:c.4-129G>A NP_005092.1:n.4-129G>A
NM_005101.4:c.4-129G>A MANE Select NP_005092.1:n.4-129G>A
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