Canonical Allele Identifier: CA230605969

Gene:

Linked Data

• dbSNP Id: rs568627240
• gnomAD v2: 11-128740740-A-T
• gnomAD v3: 11-128870845-A-T
• gnomAD v4: 11-128870845-A-T
• MyVariant Identifiers: chr11:g.128740740A>T (hg19) ; chr11:g.128870845A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128870845A>T , CM000673.2:g.128870845A>T	GRCh38
NC_000011.9:g.128740740A>T , CM000673.1:g.128740740A>T	GRCh37
NC_000011.8:g.128245950A>T	NCBI36
NG_009379.1:g.1529T>A

Transcript Alleles

HGVS	Amino-acid Change
XR_948172.1:n.6066T>A
XR_948173.1:n.5755T>A