Canonical Allele Identifier: CA1207016703

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635950T= , CM000663.2:g.171635950T= GRCh38
NC_000001.10:g.171605090T= , CM000663.1:g.171605090T= GRCh37
NC_000001.9:g.169871713T= NCBI36
NG_008859.1:g.21684A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1490A= (MYOC) MANE Select ENSP00000037502.5:p.Tyr497=
ENST00000637303.1:c.235-2680T= (MYOCOS) ENSP00000490048.1:n.235-2680T=
ENST00000638471.1:c.*828A= (MYOC) ENSP00000491206.1:n.*828A=
ENST00000037502.10:c.1490A= (MYOC) ENSP00000037502.5:p.Tyr497=
ENST00000614688.1:c.*454A= (MYOC) ENSP00000478680.1:n.*454A=
NM_000261.1:c.1490A= (MYOC) NP_000252.1:p.Tyr497=
NM_000261.2:c.1490A= (MYOC) MANE Select NP_000252.1:p.Tyr497=