Canonical Allele Identifier: CA665341648

Gene:

Linked Data

• dbSNP Id: rs1361190068
• gnomAD v3: 10-43318604-A-G
• gnomAD v4: 10-43318604-A-G
• MyVariant Identifiers: chr10:g.43814052A>G (hg19) ; chr10:g.43318604A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43318604A>G , CM000672.2:g.43318604A>G	GRCh38
NC_000010.10:g.43814052A>G , CM000672.1:g.43814052A>G	GRCh37
NC_000010.9:g.43134058A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_945902.1:n.108+9A>G
XR_945902.2:n.198+9A>G