Canonical Allele Identifier: CA62694766
Gene: STAT1 HGNC NCBI

Linked Data

dbSNP Id: rs948594082
MyVariant Identifiers: chr2:g.191014784C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191014784C>G , CM000664.2:g.191014784C>G GRCh38
NC_000002.11:g.191879510C>G , CM000664.1:g.191879510C>G GRCh37
NC_000002.10:g.191587755C>G NCBI36
NG_008294.1:g.4467G>C , LRG_111:g.4467G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000432058.1:c.-155-1106G>C ENSP00000416019.1:n.-155-1106G>C
ENST00000454414.5:c.-1-4780G>C ENSP00000411398.1:n.-1-4780G>C