Canonical Allele Identifier: CA1207016573

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635584G= , CM000663.2:g.171635584G= GRCh38
NC_000001.10:g.171604724G= , CM000663.1:g.171604724G= GRCh37
NC_000001.9:g.169871347G= NCBI36
NG_008859.1:g.22050C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*341C= (MYOC) MANE Select ENSP00000037502.5:n.*341C=
ENST00000637303.1:c.235-3046G= (MYOCOS) ENSP00000490048.1:n.235-3046G=
ENST00000638471.1:c.*1194C= (MYOC) ENSP00000491206.1:n.*1194C=
ENST00000037502.10:c.*341C= (MYOC) ENSP00000037502.5:n.*341C=
ENST00000614688.1:c.*820C= (MYOC) ENSP00000478680.1:n.*820C=
NM_000261.1:c.*341C= (MYOC) NP_000252.1:n.*341C=
NM_000261.2:c.*341C= (MYOC) MANE Select NP_000252.1:n.*341C=