Canonical Allele Identifier: CA2838514577
Gene: MYOM2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.2063006C>T , CM000670.2:g.2063006C>T GRCh38
NC_000008.9:g.1998533C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262113.9:c.653+3761C>T MANE Select ENSP00000262113.4:n.653+3761C>T
ENST00000262113.8:c.653+3761C>T ENSP00000262113.4:n.653+3761C>T
ENST00000523438.1:c.-82+17838C>T ENSP00000428396.1:n.-82+17838C>T
NM_003970.3:c.653+3761C>T NP_003961.3:n.653+3761C>T
XM_006716237.1:c.653+3761C>T XP_006716300.1:n.653+3761C>T
NM_003970.4:c.653+3761C>T MANE Select NP_003961.3:n.653+3761C>T
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