Canonical Allele Identifier: CA343725673

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636553C>G , CM000663.2:g.171636553C>G GRCh38
NC_000001.10:g.171605693C>G , CM000663.1:g.171605693C>G GRCh37
NC_000001.9:g.169872316C>G NCBI36
NG_008859.1:g.21081G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.887G>C (MYOC) MANE Select ENSP00000037502.5:p.Arg296Pro
ENST00000637303.1:c.235-2077C>G (MYOCOS) ENSP00000490048.1:n.235-2077C>G
ENST00000638471.1:c.*225G>C (MYOC) ENSP00000491206.1:n.*225G>C
ENST00000037502.10:c.887G>C (MYOC) ENSP00000037502.5:p.Arg296Pro
ENST00000614688.1:c.887G>C (MYOC) ENSP00000478680.1:p.Arg296Pro
NM_000261.1:c.887G>C (MYOC) NP_000252.1:p.Arg296Pro
NM_000261.2:c.887G>C (MYOC) MANE Select NP_000252.1:p.Arg296Pro