Canonical Allele Identifier: CA225652654

Gene:

Linked Data

• dbSNP Id: rs1023729670
• gnomAD v2: 11-80562744-A-T
• gnomAD v3: 11-80851701-A-T
• gnomAD v4: 11-80851701-A-T
• MyVariant Identifiers: chr11:g.80562744A>T (hg19) ; chr11:g.80851701A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.80851701A>T , CM000673.2:g.80851701A>T	GRCh38
NC_000011.9:g.80562744A>T , CM000673.1:g.80562744A>T	GRCh37
NC_000011.8:g.80240392A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247272.2:n.124+60590T>A