Canonical Allele Identifier: CA1207016583

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635608G= , CM000663.2:g.171635608G= GRCh38
NC_000001.10:g.171604748G= , CM000663.1:g.171604748G= GRCh37
NC_000001.9:g.169871371G= NCBI36
NG_008859.1:g.22026C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*317C= (MYOC) MANE Select ENSP00000037502.5:n.*317C=
ENST00000637303.1:c.235-3022G= (MYOCOS) ENSP00000490048.1:n.235-3022G=
ENST00000638471.1:c.*1170C= (MYOC) ENSP00000491206.1:n.*1170C=
ENST00000037502.10:c.*317C= (MYOC) ENSP00000037502.5:n.*317C=
ENST00000614688.1:c.*796C= (MYOC) ENSP00000478680.1:n.*796C=
NM_000261.1:c.*317C= (MYOC) NP_000252.1:n.*317C=
NM_000261.2:c.*317C= (MYOC) MANE Select NP_000252.1:n.*317C=