Canonical Allele Identifier: CA230605995

Gene:

Linked Data

• dbSNP Id: rs79973597
• gnomAD v3: 11-128870929-G-A
• gnomAD v4: 11-128870929-G-A
• MyVariant Identifiers: chr11:g.128740824G>A (hg19) ; chr11:g.128870929G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.128870929G>A , CM000673.2:g.128870929G>A	GRCh38
NC_000011.9:g.128740824G>A , CM000673.1:g.128740824G>A	GRCh37
NC_000011.8:g.128246034G>A	NCBI36
NG_009379.1:g.1445C>T

Transcript Alleles

HGVS	Amino-acid Change
XR_948172.1:n.5982C>T
XR_948173.1:n.5671C>T