Canonical Allele Identifier: CA337803811

Gene: ISG15

Linked Data

• dbSNP Id: rs1422581357
• gnomAD v2: 1-949476-A-G
• gnomAD v4: 1-1014096-A-G
• MyVariant Identifiers: chr1:g.949476A>G (hg19) ; chr1:g.1014096A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1014096A>G , CM000663.2:g.1014096A>G	GRCh38
NC_000001.10:g.949476A>G , CM000663.1:g.949476A>G	GRCh37
NC_000001.9:g.939339A>G	NCBI36
NG_033033.1:g.5630A>G
NG_033033.2:g.17959A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000624697.4:c.92A>G	ENSP00000485643.1:p.His31Arg
ENST00000649529.1:c.116A>G MANE Select	ENSP00000496832.1:p.His39Arg
ENST00000379389.4:c.116A>G	ENSP00000368699.4:p.His39Arg
ENST00000624652.1:c.92A>G	ENSP00000485313.1:p.His31Arg
ENST00000624697.3:c.92A>G	ENSP00000485643.1:p.His31Arg
NM_005101.3:c.116A>G	NP_005092.1:p.His39Arg
NM_005101.4:c.116A>G MANE Select	NP_005092.1:p.His39Arg