Canonical Allele Identifier: CA16724875
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs568580969
gnomAD v3: 1-1013892-C-G
gnomAD v4: 1-1013892-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013892C>G , CM000663.2:g.1013892C>G GRCh38
NC_000001.10:g.949272C>G , CM000663.1:g.949272C>G GRCh37
NC_000001.9:g.939135C>G NCBI36
NG_033033.1:g.5426C>G
NG_033033.2:g.17755C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-92C>G ENSP00000485643.1:n.-21-92C>G
ENST00000649529.1:c.4-92C>G MANE Select ENSP00000496832.1:n.4-92C>G
ENST00000379389.4:c.4-92C>G ENSP00000368699.4:n.4-92C>G
ENST00000624652.1:c.-21-92C>G ENSP00000485313.1:n.-21-92C>G
ENST00000624697.3:c.-21-92C>G ENSP00000485643.1:n.-21-92C>G
NM_005101.3:c.4-92C>G NP_005092.1:n.4-92C>G
NM_005101.4:c.4-92C>G MANE Select NP_005092.1:n.4-92C>G