Canonical Allele Identifier: CA1207016681

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635885G= , CM000663.2:g.171635885G= GRCh38
NC_000001.10:g.171605025G= , CM000663.1:g.171605025G= GRCh37
NC_000001.9:g.169871648G= NCBI36
NG_008859.1:g.21749C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*40C= (MYOC) MANE Select ENSP00000037502.5:n.*40C=
ENST00000637303.1:c.235-2745G= (MYOCOS) ENSP00000490048.1:n.235-2745G=
ENST00000638471.1:c.*893C= (MYOC) ENSP00000491206.1:n.*893C=
ENST00000037502.10:c.*40C= (MYOC) ENSP00000037502.5:n.*40C=
ENST00000614688.1:c.*519C= (MYOC) ENSP00000478680.1:n.*519C=
NM_000261.1:c.*40C= (MYOC) NP_000252.1:n.*40C=
NM_000261.2:c.*40C= (MYOC) MANE Select NP_000252.1:n.*40C=