Canonical Allele Identifier: CA997657499
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs1570110747
gnomAD v3: 1-1013895-G-A
gnomAD v4: 1-1013895-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013895G>A , CM000663.2:g.1013895G>A GRCh38
NC_000001.10:g.949275G>A , CM000663.1:g.949275G>A GRCh37
NC_000001.9:g.939138G>A NCBI36
NG_033033.1:g.5429G>A
NG_033033.2:g.17758G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-89G>A ENSP00000485643.1:n.-21-89G>A
ENST00000649529.1:c.4-89G>A MANE Select ENSP00000496832.1:n.4-89G>A
ENST00000379389.4:c.4-89G>A ENSP00000368699.4:n.4-89G>A
ENST00000624652.1:c.-21-89G>A ENSP00000485313.1:n.-21-89G>A
ENST00000624697.3:c.-21-89G>A ENSP00000485643.1:n.-21-89G>A
NM_005101.3:c.4-89G>A NP_005092.1:n.4-89G>A
NM_005101.4:c.4-89G>A MANE Select NP_005092.1:n.4-89G>A
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