Canonical Allele Identifier: CA473651125

Gene:

Linked Data

• dbSNP Id: rs1409094486
• gnomAD v2: 11-27505636-A-T
• gnomAD v3: 11-27484089-A-T
• gnomAD v4: 11-27484089-A-T
• MyVariant Identifiers: chr11:g.27505636A>T (hg19) ; chr11:g.27484089A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27484089A>T , CM000673.2:g.27484089A>T	GRCh38
NC_000011.9:g.27505636A>T , CM000673.1:g.27505636A>T	GRCh37
NC_000011.8:g.27462212A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496450.1:n.240A>T