Canonical Allele Identifier: CA1670153003
Gene: EPM2A HGNC NCBI

Linked Data

dbSNP Id: rs1779086359

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.145443056A>G , CM000668.2:g.145443056A>G GRCh38
NC_000006.11:g.145764192A>G , CM000668.1:g.145764192A>G GRCh37
NC_000006.10:g.145805885A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000638717.1:c.556-58959T>C
XM_024446550.1:c.773-58959T>C XP_024302318.1:n.773-58959T>C