Canonical Allele Identifier: CA343726196

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636666T>A , CM000663.2:g.171636666T>A GRCh38
NC_000001.10:g.171605806T>A , CM000663.1:g.171605806T>A GRCh37
NC_000001.9:g.169872429T>A NCBI36
NG_008859.1:g.20968A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.774A>T (MYOC) MANE Select ENSP00000037502.5:p.Arg258Ser
ENST00000637303.1:c.235-1964T>A (MYOCOS) ENSP00000490048.1:n.235-1964T>A
ENST00000638471.1:c.*112A>T (MYOC) ENSP00000491206.1:n.*112A>T
ENST00000037502.10:c.774A>T (MYOC) ENSP00000037502.5:p.Arg258Ser
ENST00000614688.1:c.774A>T (MYOC) ENSP00000478680.1:p.Arg258Ser
NM_000261.1:c.774A>T (MYOC) NP_000252.1:p.Arg258Ser
NM_000261.2:c.774A>T (MYOC) MANE Select NP_000252.1:p.Arg258Ser