Canonical Allele Identifier: CA762423262
Gene: STAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1432590190
MyVariant Identifiers: chr2:g.191879443C>T (hg19) chr2:g.191014717C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191014717C>T , CM000664.2:g.191014717C>T GRCh38
NC_000002.11:g.191879443C>T , CM000664.1:g.191879443C>T GRCh37
NC_000002.10:g.191587688C>T NCBI36
NG_008294.1:g.4534G>A , LRG_111:g.4534G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000432058.1:c.-155-1039G>A ENSP00000416019.1:n.-155-1039G>A
ENST00000454414.5:c.-1-4713G>A ENSP00000411398.1:n.-1-4713G>A
Search 100 bp 5'
Search 100 bp 3'