Canonical Allele Identifier: CA507636
Gene: ISG15 HGNC NCBI

Linked Data

ClinVar Variation Id: 957804
ClinVar RCV Id: RCV001230855 RCV002563748
dbSNP Id: rs139516378
ExAC: 1:949511 G / A
gnomAD v2: 1-949511-G-A
gnomAD v3: 1-1014131-G-A
gnomAD v4: 1-1014131-G-A
MyVariant Identifiers: chr1:g.949511G>A (hg19) chr1:g.1014131G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014131G>A , CM000663.2:g.1014131G>A GRCh38
NC_000001.10:g.949511G>A , CM000663.1:g.949511G>A GRCh37
NC_000001.9:g.939374G>A NCBI36
NG_033033.1:g.5665G>A
NG_033033.2:g.17994G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000624697.4:c.127G>A ENSP00000485643.1:p.Gly43Ser
ENST00000649529.1:c.151G>A MANE Select ENSP00000496832.1:p.Gly51Ser
ENST00000379389.4:c.151G>A ENSP00000368699.4:p.Gly51Ser
ENST00000624652.1:c.127G>A ENSP00000485313.1:p.Gly43Ser
ENST00000624697.3:c.127G>A ENSP00000485643.1:p.Gly43Ser
NM_005101.3:c.151G>A NP_005092.1:p.Gly51Ser
NM_005101.4:c.151G>A MANE Select NP_005092.1:p.Gly51Ser
Search 100 bp 5'
Search 100 bp 3'