Canonical Allele Identifier: CA211666063

Gene:

Linked Data

• dbSNP Id: rs935243151
• gnomAD v4: 10-94762596-G-A
• MyVariant Identifiers: chr10:g.96522353G>A (hg19) ; chr10:g.94762596G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762596G>A , CM000672.2:g.94762596G>A	GRCh38
NC_000010.10:g.96522353G>A , CM000672.1:g.96522353G>A	GRCh37
NC_000010.9:g.96512343G>A	NCBI36
NG_008384.2:g.4891G>A
NG_008384.3:g.4916G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000464755.1:c.932-12462G>A	ENSP00000483243.1:n.932-12462G>A