Canonical Allele Identifier: CA1207016610

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635720A= , CM000663.2:g.171635720A= GRCh38
NC_000001.10:g.171604860A= , CM000663.1:g.171604860A= GRCh37
NC_000001.9:g.169871483A= NCBI36
NG_008859.1:g.21914T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*205T= (MYOC) MANE Select ENSP00000037502.5:n.*205T=
ENST00000637303.1:c.235-2910A= (MYOCOS) ENSP00000490048.1:n.235-2910A=
ENST00000638471.1:c.*1058T= (MYOC) ENSP00000491206.1:n.*1058T=
ENST00000037502.10:c.*205T= (MYOC) ENSP00000037502.5:n.*205T=
ENST00000614688.1:c.*684T= (MYOC) ENSP00000478680.1:n.*684T=
NM_000261.1:c.*205T= (MYOC) NP_000252.1:n.*205T=
NM_000261.2:c.*205T= (MYOC) MANE Select NP_000252.1:n.*205T=