Canonical Allele Identifier: CA476840468

Gene:

Linked Data

• dbSNP Id: rs1945833792
• gnomAD v3: 11-114360683-A-T
• gnomAD v4: 11-114360683-A-T
• MyVariant Identifiers: chr11:g.114231405A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.114360683A>T , CM000673.2:g.114360683A>T	GRCh38
NC_000011.9:g.114231405A>T , CM000673.1:g.114231405A>T	GRCh37
NC_000011.8:g.113736615A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120567.1:n.3783T>A