Canonical Allele Identifier: CA343723405

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636041A>G , CM000663.2:g.171636041A>G GRCh38
NC_000001.10:g.171605181A>G , CM000663.1:g.171605181A>G GRCh37
NC_000001.9:g.169871804A>G NCBI36
NG_008859.1:g.21593T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1399T>C (MYOC) MANE Select ENSP00000037502.5:p.Phe467Leu
ENST00000637303.1:c.235-2589A>G (MYOCOS) ENSP00000490048.1:n.235-2589A>G
ENST00000638471.1:c.*737T>C (MYOC) ENSP00000491206.1:n.*737T>C
ENST00000037502.10:c.1399T>C (MYOC) ENSP00000037502.5:p.Phe467Leu
ENST00000614688.1:c.*363T>C (MYOC) ENSP00000478680.1:n.*363T>C
NM_000261.1:c.1399T>C (MYOC) NP_000252.1:p.Phe467Leu
NM_000261.2:c.1399T>C (MYOC) MANE Select NP_000252.1:p.Phe467Leu