Canonical Allele Identifier: CA228717389

Gene:

Linked Data

• dbSNP Id: rs902084521
• gnomAD v3: 11-114360682-T-C
• gnomAD v4: 11-114360682-T-C
• MyVariant Identifiers: chr11:g.114231404T>C (hg19) ; chr11:g.114360682T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.114360682T>C , CM000673.2:g.114360682T>C	GRCh38
NC_000011.9:g.114231404T>C , CM000673.1:g.114231404T>C	GRCh37
NC_000011.8:g.113736614T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120567.1:n.3784A>G