Canonical Allele Identifier: CA884553519
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs1299970354
gnomAD v4: 1-1013874-C-G
MyVariant Identifiers: chr1:g.949254C>G (hg19) chr1:g.1013874C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013874C>G , CM000663.2:g.1013874C>G GRCh38
NC_000001.10:g.949254C>G , CM000663.1:g.949254C>G GRCh37
NC_000001.9:g.939117C>G NCBI36
NG_033033.1:g.5408C>G
NG_033033.2:g.17737C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-110C>G ENSP00000485643.1:n.-21-110C>G
ENST00000649529.1:c.4-110C>G MANE Select ENSP00000496832.1:n.4-110C>G
ENST00000379389.4:c.4-110C>G ENSP00000368699.4:n.4-110C>G
ENST00000624652.1:c.-21-110C>G ENSP00000485313.1:n.-21-110C>G
ENST00000624697.3:c.-21-110C>G ENSP00000485643.1:n.-21-110C>G
NM_005101.3:c.4-110C>G NP_005092.1:n.4-110C>G
NM_005101.4:c.4-110C>G MANE Select NP_005092.1:n.4-110C>G
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