Canonical Allele Identifier: CA1207016593

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635637C= , CM000663.2:g.171635637C= GRCh38
NC_000001.10:g.171604777C= , CM000663.1:g.171604777C= GRCh37
NC_000001.9:g.169871400C= NCBI36
NG_008859.1:g.21997G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*288G= (MYOC) MANE Select ENSP00000037502.5:n.*288G=
ENST00000637303.1:c.235-2993C= (MYOCOS) ENSP00000490048.1:n.235-2993C=
ENST00000638471.1:c.*1141G= (MYOC) ENSP00000491206.1:n.*1141G=
ENST00000037502.10:c.*288G= (MYOC) ENSP00000037502.5:n.*288G=
ENST00000614688.1:c.*767G= (MYOC) ENSP00000478680.1:n.*767G=
NM_000261.1:c.*288G= (MYOC) NP_000252.1:n.*288G=
NM_000261.2:c.*288G= (MYOC) MANE Select NP_000252.1:n.*288G=