Canonical Allele Identifier: CA766892664

Gene: CAPN10

Linked Data

• dbSNP Id: rs5030952
• MyVariant Identifiers: chr2:g.241542703C>G (hg19) ; chr2:g.240603286C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240603286C>G , CM000664.2:g.240603286C>G	GRCh38
NC_000002.11:g.241542703C>G , CM000664.1:g.241542703C>G	GRCh37
NC_000002.10:g.241191376C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000270364.11:c.274-13102C>G	ENSP00000270364.7:n.274-13102C>G
ENST00000426297.1:c.167-3101C>G