Canonical Allele Identifier: CA1244202

Linked Data

ClinVar Variation Id: 875084
dbSNP Id: rs200547613

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171638675C>T , CM000663.2:g.171638675C>T GRCh38
NC_000001.10:g.171607815C>T , CM000663.1:g.171607815C>T GRCh37
NC_000001.9:g.169874438C>T NCBI36
NG_008859.1:g.18959G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.652G>A (MYOC) MANE Select ENSP00000037502.5:p.Glu218Lys
ENST00000637303.1:c.280C>T (MYOCOS) ENSP00000490048.1:p.Arg94Trp
ENST00000638471.1:c.182G>A (MYOC) ENSP00000491206.1:p.Arg61Gln
ENST00000037502.10:c.652G>A (MYOC) ENSP00000037502.5:p.Glu218Lys
ENST00000614688.1:c.652G>A (MYOC) ENSP00000478680.1:p.Glu218Lys
NM_000261.1:c.652G>A (MYOC) NP_000252.1:p.Glu218Lys
NM_000261.2:c.652G>A (MYOC) MANE Select NP_000252.1:p.Glu218Lys