Canonical Allele Identifier: CA211666120

Gene:

Linked Data

• dbSNP Id: rs754719717
• MyVariant Identifiers: chr10:g.96522373A>G (hg19) ; chr10:g.94762616A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762616A>G , CM000672.2:g.94762616A>G	GRCh38
NC_000010.10:g.96522373A>G , CM000672.1:g.96522373A>G	GRCh37
NC_000010.9:g.96512363A>G	NCBI36
NG_008384.2:g.4911A>G
NG_008384.3:g.4936A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000464755.1:c.932-12442A>G	ENSP00000483243.1:n.932-12442A>G