Canonical Allele Identifier: CA436706667
Gene: SI HGNC NCBI

Linked Data

COSMIC: COSM1291640
MyVariant Identifiers: chr3:g.164764698A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165046910A>T , CM000665.2:g.165046910A>T GRCh38
NC_000003.11:g.164764698A>T , CM000665.1:g.164764698A>T GRCh37
NC_000003.10:g.166247392A>T NCBI36
NG_017043.1:g.36586T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264382.8:c.1818T>A MANE Select ENSP00000264382.3:p.Thr606=
ENST00000264382.7:c.1818T>A ENSP00000264382.3:p.Thr606=
NM_001041.3:c.1818T>A NP_001032.2:p.Thr606=
XM_011513078.1:c.1719T>A XP_011511380.1:p.Thr573=
XM_011513078.2:c.1719T>A XP_011511380.1:p.Thr573=
NM_001041.4:c.1818T>A MANE Select NP_001032.2:p.Thr606=
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