Canonical Allele Identifier: CA476175851

Gene:

Linked Data

• gnomAD v4: 11-89733575-C-T
• MyVariant Identifiers: chr11:g.89466743C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89733575C>T , CM000673.2:g.89733575C>T	GRCh38
NC_000011.9:g.89466743C>T , CM000673.1:g.89466743C>T	GRCh37
NC_000011.8:g.89106391C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000527668.1:n.2559C>T