Canonical Allele Identifier: CA355029979
Gene: SI HGNC NCBI

Linked Data

gnomAD v4: 3-164996748-C-G
MyVariant Identifiers: chr3:g.164714536C>G (hg19) chr3:g.164996748C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.164996748C>G , CM000665.2:g.164996748C>G GRCh38
NC_000003.11:g.164714536C>G , CM000665.1:g.164714536C>G GRCh37
NC_000003.10:g.166197230C>G NCBI36
NG_017043.1:g.86748G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264382.8:c.4565G>C MANE Select ENSP00000264382.3:p.Gly1522Ala
ENST00000264382.7:c.4565G>C ENSP00000264382.3:p.Gly1522Ala
NM_001041.3:c.4565G>C NP_001032.2:p.Gly1522Ala
XM_011513078.1:c.4466G>C XP_011511380.1:p.Gly1489Ala
XM_011513078.2:c.4466G>C XP_011511380.1:p.Gly1489Ala
NM_001041.4:c.4565G>C MANE Select NP_001032.2:p.Gly1522Ala
Search 100 bp 5'
Search 100 bp 3'