Canonical Allele Identifier: CA602555867

Gene:

Linked Data

• gnomAD v2: 11-128325329-C-G
• gnomAD v3: 11-128455434-C-G
• gnomAD v4: 11-128455434-C-G
• MyVariant Identifiers: chr11:g.128325329C>G (hg19) ; chr11:g.128455434C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128455434C>G , CM000673.2:g.128455434C>G	GRCh38
NC_000011.9:g.128325329C>G , CM000673.1:g.128325329C>G	GRCh37
NC_000011.8:g.127830539C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_948164.1:n.4154C>G
XR_948165.1:n.3467+687C>G