Canonical Allele Identifier: CA337804669
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs1429823613
gnomAD v2: 1-949621-G-C
gnomAD v3: 1-1014241-G-C
gnomAD v4: 1-1014241-G-C
MyVariant Identifiers: chr1:g.949621G>C (hg19) chr1:g.1014241G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014241G>C , CM000663.2:g.1014241G>C GRCh38
NC_000001.10:g.949621G>C , CM000663.1:g.949621G>C GRCh37
NC_000001.9:g.939484G>C NCBI36
NG_033033.1:g.5775G>C
NG_033033.2:g.18104G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.237G>C ENSP00000485643.1:p.Arg79Ser
ENST00000649529.1:c.261G>C MANE Select ENSP00000496832.1:p.Arg87Ser
ENST00000379389.4:c.261G>C ENSP00000368699.4:p.Arg87Ser
ENST00000624652.1:c.237G>C ENSP00000485313.1:p.Arg79Ser
ENST00000624697.3:c.237G>C ENSP00000485643.1:p.Arg79Ser
NM_005101.3:c.261G>C NP_005092.1:p.Arg87Ser
NM_005101.4:c.261G>C MANE Select NP_005092.1:p.Arg87Ser
Search 100 bp 5'
Search 100 bp 3'