Canonical Allele Identifier: CA16724818
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs552336577
gnomAD v2: 1-949206-A-G
gnomAD v3: 1-1013826-A-G
gnomAD v4: 1-1013826-A-G
MyVariant Identifiers: chr1:g.949206A>G (hg19) chr1:g.1013826A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013826A>G , CM000663.2:g.1013826A>G GRCh38
NC_000001.10:g.949206A>G , CM000663.1:g.949206A>G GRCh37
NC_000001.9:g.939069A>G NCBI36
NG_033033.1:g.5360A>G
NG_033033.2:g.17689A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-158A>G ENSP00000485643.1:n.-21-158A>G
ENST00000649529.1:c.4-158A>G MANE Select ENSP00000496832.1:n.4-158A>G
ENST00000379389.4:c.4-158A>G ENSP00000368699.4:n.4-158A>G
ENST00000624652.1:c.-21-158A>G ENSP00000485313.1:n.-21-158A>G
ENST00000624697.3:c.-21-158A>G ENSP00000485643.1:n.-21-158A>G
NM_005101.3:c.4-158A>G NP_005092.1:n.4-158A>G
NM_005101.4:c.4-158A>G MANE Select NP_005092.1:n.4-158A>G
Search 100 bp 5'
Search 100 bp 3'