Canonical Allele Identifier: CA343727107

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171638703G>T , CM000663.2:g.171638703G>T GRCh38
NC_000001.10:g.171607843G>T , CM000663.1:g.171607843G>T GRCh37
NC_000001.9:g.169874466G>T NCBI36
NG_008859.1:g.18931C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.624C>A (MYOC) MANE Select ENSP00000037502.5:p.Asp208Glu
ENST00000637303.1:c.308G>T (MYOCOS) ENSP00000490048.1:p.Cys103Phe
ENST00000638471.1:c.154C>A (MYOC) ENSP00000491206.1:p.His52Asn
ENST00000037502.10:c.624C>A (MYOC) ENSP00000037502.5:p.Asp208Glu
ENST00000614688.1:c.624C>A (MYOC) ENSP00000478680.1:p.Asp208Glu
NM_000261.1:c.624C>A (MYOC) NP_000252.1:p.Asp208Glu
NM_000261.2:c.624C>A (MYOC) MANE Select NP_000252.1:p.Asp208Glu