Canonical Allele Identifier: CA1207016626

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635752C= , CM000663.2:g.171635752C= GRCh38
NC_000001.10:g.171604892C= , CM000663.1:g.171604892C= GRCh37
NC_000001.9:g.169871515C= NCBI36
NG_008859.1:g.21882G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*173G= (MYOC) MANE Select ENSP00000037502.5:n.*173G=
ENST00000637303.1:c.235-2878C= (MYOCOS) ENSP00000490048.1:n.235-2878C=
ENST00000638471.1:c.*1026G= (MYOC) ENSP00000491206.1:n.*1026G=
ENST00000037502.10:c.*173G= (MYOC) ENSP00000037502.5:n.*173G=
ENST00000614688.1:c.*652G= (MYOC) ENSP00000478680.1:n.*652G=
NM_000261.1:c.*173G= (MYOC) NP_000252.1:n.*173G=
NM_000261.2:c.*173G= (MYOC) MANE Select NP_000252.1:n.*173G=