Canonical Allele Identifier: CA1207023295
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652647T= , CM000663.2:g.171652647T= GRCh38
NC_000001.10:g.171621787T= , CM000663.1:g.171621787T= GRCh37
NC_000001.9:g.169888410T= NCBI36
NG_008859.1:g.4987A=

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.-36A= MANE Select ENSP00000037502.5:n.-36A=
ENST00000037502.10:c.-36A= ENSP00000037502.5:n.-36A=
NM_000261.2:c.-36A= MANE Select NP_000252.1:n.-36A=