Canonical Allele Identifier: CA1207016630

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635756A= , CM000663.2:g.171635756A= GRCh38
NC_000001.10:g.171604896A= , CM000663.1:g.171604896A= GRCh37
NC_000001.9:g.169871519A= NCBI36
NG_008859.1:g.21878T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*169T= (MYOC) MANE Select ENSP00000037502.5:n.*169T=
ENST00000637303.1:c.235-2874A= (MYOCOS) ENSP00000490048.1:n.235-2874A=
ENST00000638471.1:c.*1022T= (MYOC) ENSP00000491206.1:n.*1022T=
ENST00000037502.10:c.*169T= (MYOC) ENSP00000037502.5:n.*169T=
ENST00000614688.1:c.*648T= (MYOC) ENSP00000478680.1:n.*648T=
NM_000261.1:c.*169T= (MYOC) NP_000252.1:n.*169T=
NM_000261.2:c.*169T= (MYOC) MANE Select NP_000252.1:n.*169T=