Canonical Allele Identifier: CA415756822
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs151259752
MyVariant Identifiers: chr1:g.949579G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1014199G>C , CM000663.2:g.1014199G>C GRCh38
NC_000001.10:g.949579G>C , CM000663.1:g.949579G>C GRCh37
NC_000001.9:g.939442G>C NCBI36
NG_033033.1:g.5733G>C
NG_033033.2:g.18062G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.195G>C ENSP00000485643.1:p.Leu65=
ENST00000649529.1:c.219G>C MANE Select ENSP00000496832.1:p.Leu73=
ENST00000379389.4:c.219G>C ENSP00000368699.4:p.Leu73=
ENST00000624652.1:c.195G>C ENSP00000485313.1:p.Leu65=
ENST00000624697.3:c.195G>C ENSP00000485643.1:p.Leu65=
NM_005101.3:c.219G>C NP_005092.1:p.Leu73=
NM_005101.4:c.219G>C MANE Select NP_005092.1:p.Leu73=
Search 100 bp 5'
Search 100 bp 3'