Canonical Allele Identifier: CA436706661
Gene: SI HGNC NCBI

Linked Data

dbSNP Id: rs199885741
MyVariant Identifiers: chr3:g.164764692T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.165046904T>C , CM000665.2:g.165046904T>C GRCh38
NC_000003.11:g.164764692T>C , CM000665.1:g.164764692T>C GRCh37
NC_000003.10:g.166247386T>C NCBI36
NG_017043.1:g.36592A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264382.8:c.1824A>G MANE Select ENSP00000264382.3:p.Ser608=
ENST00000264382.7:c.1824A>G ENSP00000264382.3:p.Ser608=
NM_001041.3:c.1824A>G NP_001032.2:p.Ser608=
XM_011513078.1:c.1725A>G XP_011511380.1:p.Ser575=
XM_011513078.2:c.1725A>G XP_011511380.1:p.Ser575=
NM_001041.4:c.1824A>G MANE Select NP_001032.2:p.Ser608=
Search 100 bp 5'
Search 100 bp 3'