Canonical Allele Identifier: CA337803696
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs1219350132
gnomAD v3: 1-1014074-A-G
gnomAD v4: 1-1014074-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014074A>G , CM000663.2:g.1014074A>G GRCh38
NC_000001.10:g.949454A>G , CM000663.1:g.949454A>G GRCh37
NC_000001.9:g.939317A>G NCBI36
NG_033033.1:g.5608A>G
NG_033033.2:g.17937A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.70A>G ENSP00000485643.1:p.Ile24Val
ENST00000649529.1:c.94A>G MANE Select ENSP00000496832.1:p.Ile32Val
ENST00000379389.4:c.94A>G ENSP00000368699.4:p.Ile32Val
ENST00000624652.1:c.70A>G ENSP00000485313.1:p.Ile24Val
ENST00000624697.3:c.70A>G ENSP00000485643.1:p.Ile24Val
NM_005101.3:c.94A>G NP_005092.1:p.Ile32Val
NM_005101.4:c.94A>G MANE Select NP_005092.1:p.Ile32Val