Canonical Allele Identifier: CA476175847

Gene:

Linked Data

• gnomAD v4: 11-89733574-T-C
• MyVariant Identifiers: chr11:g.89466742T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89733574T>C , CM000673.2:g.89733574T>C	GRCh38
NC_000011.9:g.89466742T>C , CM000673.1:g.89466742T>C	GRCh37
NC_000011.8:g.89106390T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000527668.1:n.2558T>C