Canonical Allele Identifier: CA520623814
Gene: ISG15 HGNC NCBI

Linked Data

dbSNP Id: rs1254377336
gnomAD v2: 1-949293-G-A
gnomAD v3: 1-1013913-G-A
gnomAD v4: 1-1013913-G-A
MyVariant Identifiers: chr1:g.949293G>A (hg19) chr1:g.1013913G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1013913G>A , CM000663.2:g.1013913G>A GRCh38
NC_000001.10:g.949293G>A , CM000663.1:g.949293G>A GRCh37
NC_000001.9:g.939156G>A NCBI36
NG_033033.1:g.5447G>A
NG_033033.2:g.17776G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000624697.4:c.-21-71G>A ENSP00000485643.1:n.-21-71G>A
ENST00000649529.1:c.4-71G>A MANE Select ENSP00000496832.1:n.4-71G>A
ENST00000379389.4:c.4-71G>A ENSP00000368699.4:n.4-71G>A
ENST00000624652.1:c.-21-71G>A ENSP00000485313.1:n.-21-71G>A
ENST00000624697.3:c.-21-71G>A ENSP00000485643.1:n.-21-71G>A
NM_005101.3:c.4-71G>A NP_005092.1:n.4-71G>A
NM_005101.4:c.4-71G>A MANE Select NP_005092.1:n.4-71G>A
Search 100 bp 5'
Search 100 bp 3'