Canonical Allele Identifier: CA68139543
Gene: CAPN10 HGNC NCBI

Linked Data

dbSNP Id: rs946621221
MyVariant Identifiers: chr2:g.241542644C>T (hg19) chr2:g.240603227C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240603227C>T , CM000664.2:g.240603227C>T GRCh38
NC_000002.11:g.241542644C>T , CM000664.1:g.241542644C>T GRCh37
NC_000002.10:g.241191317C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000270364.11:c.274-13161C>T ENSP00000270364.7:n.274-13161C>T
ENST00000426297.1:c.167-3160C>T
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