Canonical Allele Identifier: CA673250494

Gene:

Linked Data

• dbSNP Id: rs1263456868
• gnomAD v3: 11-128870856-G-T
• gnomAD v4: 11-128870856-G-T
• MyVariant Identifiers: chr11:g.128740751G>T (hg19) ; chr11:g.128870856G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128870856G>T , CM000673.2:g.128870856G>T	GRCh38
NC_000011.9:g.128740751G>T , CM000673.1:g.128740751G>T	GRCh37
NC_000011.8:g.128245961G>T	NCBI36
NG_009379.1:g.1518C>A

Transcript Alleles

HGVS	Amino-acid Change
XR_948172.1:n.6055C>A
XR_948173.1:n.5744C>A