Canonical Allele Identifier: CA2746628368
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652680_171652681del , CM000663.2:g.171652680_171652681del GRCh38
NC_000001.10:g.171621820_171621821del , CM000663.1:g.171621820_171621821del GRCh37
NC_000001.9:g.169888443_169888444del NCBI36
NG_008859.1:g.4953_4954del

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.-70_-69del MANE Select ENSP00000037502.5:n.-70_-69del
ENST00000037502.10:c.-70_-69del ENSP00000037502.5:n.-70_-69del
NM_000261.2:c.-70_-69del MANE Select NP_000252.1:n.-70_-69del