Canonical Allele Identifier: CA1207016679

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635880C= , CM000663.2:g.171635880C= GRCh38
NC_000001.10:g.171605020C= , CM000663.1:g.171605020C= GRCh37
NC_000001.9:g.169871643C= NCBI36
NG_008859.1:g.21754G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*45G= (MYOC) MANE Select ENSP00000037502.5:n.*45G=
ENST00000637303.1:c.235-2750C= (MYOCOS) ENSP00000490048.1:n.235-2750C=
ENST00000638471.1:c.*898G= (MYOC) ENSP00000491206.1:n.*898G=
ENST00000037502.10:c.*45G= (MYOC) ENSP00000037502.5:n.*45G=
ENST00000614688.1:c.*524G= (MYOC) ENSP00000478680.1:n.*524G=
NM_000261.1:c.*45G= (MYOC) NP_000252.1:n.*45G=
NM_000261.2:c.*45G= (MYOC) MANE Select NP_000252.1:n.*45G=