Canonical Allele Identifier: CA337804663
Gene: ISG15 HGNC NCBI

Linked Data

gnomAD v4: 1-1014237-T-G
MyVariant Identifiers: chr1:g.949617T>G (hg19) chr1:g.1014237T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014237T>G , CM000663.2:g.1014237T>G GRCh38
NC_000001.10:g.949617T>G , CM000663.1:g.949617T>G GRCh37
NC_000001.9:g.939480T>G NCBI36
NG_033033.1:g.5771T>G
NG_033033.2:g.18100T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.233T>G ENSP00000485643.1:p.Val78Gly
ENST00000649529.1:c.257T>G MANE Select ENSP00000496832.1:p.Val86Gly
ENST00000379389.4:c.257T>G ENSP00000368699.4:p.Val86Gly
ENST00000624652.1:c.233T>G ENSP00000485313.1:p.Val78Gly
ENST00000624697.3:c.233T>G ENSP00000485643.1:p.Val78Gly
NM_005101.3:c.257T>G NP_005092.1:p.Val86Gly
NM_005101.4:c.257T>G MANE Select NP_005092.1:p.Val86Gly
Search 100 bp 5'
Search 100 bp 3'