Canonical Allele Identifier: CA762423257
Gene: STAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1158009621
MyVariant Identifiers: chr2:g.191879428C>G (hg19) chr2:g.191014702C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191014702C>G , CM000664.2:g.191014702C>G GRCh38
NC_000002.11:g.191879428C>G , CM000664.1:g.191879428C>G GRCh37
NC_000002.10:g.191587673C>G NCBI36
NG_008294.1:g.4549G>C , LRG_111:g.4549G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000432058.1:c.-155-1024G>C ENSP00000416019.1:n.-155-1024G>C
ENST00000454414.5:c.-1-4698G>C ENSP00000411398.1:n.-1-4698G>C
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