Canonical Allele Identifier: CA762423502
Gene: STAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1488055486
gnomAD v3: 2-191015715-T-A
gnomAD v4: 2-191015715-T-A
MyVariant Identifiers: chr2:g.191880441T>A (hg19) chr2:g.191015715T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191015715T>A , CM000664.2:g.191015715T>A GRCh38
NC_000002.11:g.191880441T>A , CM000664.1:g.191880441T>A GRCh37
NC_000002.10:g.191588686T>A NCBI36
NG_008294.1:g.3536A>T , LRG_111:g.3536A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000432058.1:c.-155-2037A>T ENSP00000416019.1:n.-155-2037A>T
ENST00000454414.5:c.-2+4485A>T ENSP00000411398.1:n.-2+4485A>T
Search 100 bp 5'
Search 100 bp 3'