Canonical Allele Identifier: CA220643961
Gene:

Linked Data

dbSNP Id: rs888866831
gnomAD v2: 11-34833806-T-C
gnomAD v3: 11-34812259-T-C
gnomAD v4: 11-34812259-T-C
MyVariant Identifiers: chr11:g.34833806T>C (hg19) chr11:g.34812259T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34812259T>C , CM000673.2:g.34812259T>C GRCh38
NC_000011.9:g.34833806T>C , CM000673.1:g.34833806T>C GRCh37
NC_000011.8:g.34790382T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428897.2:n.579+57652T>C
XR_931188.1:n.693+57652T>C
XR_931189.1:n.854+57652T>C
XR_931190.1:n.639+57652T>C
XR_931191.1:n.689+57652T>C
XR_001748174.1:n.855+57652T>C
XR_001748176.1:n.1016+57652T>C
XR_002957246.1:n.639+57652T>C
Search 100 bp 5'
Search 100 bp 3'