Canonical Allele Identifier: CA762423508
Gene: STAT1 HGNC NCBI

Linked Data

dbSNP Id: rs1229092407
MyVariant Identifiers: chr2:g.191880461T>C (hg19) chr2:g.191015735T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191015735T>C , CM000664.2:g.191015735T>C GRCh38
NC_000002.11:g.191880461T>C , CM000664.1:g.191880461T>C GRCh37
NC_000002.10:g.191588706T>C NCBI36
NG_008294.1:g.3516A>G , LRG_111:g.3516A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000432058.1:c.-155-2057A>G ENSP00000416019.1:n.-155-2057A>G
ENST00000454414.5:c.-2+4465A>G ENSP00000411398.1:n.-2+4465A>G
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