Canonical Allele Identifier: CA766892636
Gene: CAPN10 HGNC NCBI

Linked Data

dbSNP Id: rs1254252229
MyVariant Identifiers: chr2:g.241542636G>A (hg19) chr2:g.240603219G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240603219G>A , CM000664.2:g.240603219G>A GRCh38
NC_000002.11:g.241542636G>A , CM000664.1:g.241542636G>A GRCh37
NC_000002.10:g.241191309G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270364.11:c.274-13169G>A ENSP00000270364.7:n.274-13169G>A
ENST00000426297.1:c.167-3168G>A
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