Canonical Allele Identifier: CA343725776

Linked Data

ClinVar Variation Id: 2442268
ClinVar RCV Id: RCV003148597

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636576G>C , CM000663.2:g.171636576G>C GRCh38
NC_000001.10:g.171605716G>C , CM000663.1:g.171605716G>C GRCh37
NC_000001.9:g.169872339G>C NCBI36
NG_008859.1:g.21058C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.864C>G (MYOC) MANE Select ENSP00000037502.5:p.Ile288Met
ENST00000637303.1:c.235-2054G>C (MYOCOS) ENSP00000490048.1:n.235-2054G>C
ENST00000638471.1:c.*202C>G (MYOC) ENSP00000491206.1:n.*202C>G
ENST00000037502.10:c.864C>G (MYOC) ENSP00000037502.5:p.Ile288Met
ENST00000614688.1:c.864C>G (MYOC) ENSP00000478680.1:p.Ile288Met
NM_000261.1:c.864C>G (MYOC) NP_000252.1:p.Ile288Met
NM_000261.2:c.864C>G (MYOC) MANE Select NP_000252.1:p.Ile288Met