Canonical Allele Identifier: CA436706649

Gene: SI

Linked Data

• MyVariant Identifiers: chr3:g.164764662T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.165046874T>C , CM000665.2:g.165046874T>C	GRCh38
NC_000003.11:g.164764662T>C , CM000665.1:g.164764662T>C	GRCh37
NC_000003.10:g.166247356T>C	NCBI36
NG_017043.1:g.36622A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264382.8:c.1854A>G MANE Select	ENSP00000264382.3:p.Gly618=
ENST00000264382.7:c.1854A>G	ENSP00000264382.3:p.Gly618=
NM_001041.3:c.1854A>G	NP_001032.2:p.Gly618=
XM_011513078.1:c.1755A>G	XP_011511380.1:p.Gly585=
XM_011513078.2:c.1755A>G	XP_011511380.1:p.Gly585=
NM_001041.4:c.1854A>G MANE Select	NP_001032.2:p.Gly618=