Canonical Allele Identifier: CA602119351

Gene:

Linked Data

• gnomAD v2: 11-116313435-C-T
• MyVariant Identifiers: chr11:g.116313435C>T (hg19) ; chr11:g.116442718C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116442718C>T , CM000673.2:g.116442718C>T	GRCh38
NC_000011.9:g.116313435C>T , CM000673.1:g.116313435C>T	GRCh37
NC_000011.8:g.115818645C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_001748403.1:n.349+31159G>A