Canonical Allele Identifier: CA1244210

Linked Data

ClinVar Variation Id: 876020
dbSNP Id: rs2234927

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.624C>G (MYOC) MANE Select ENSP00000037502.5:p.Asp208Glu
ENST00000637303.1:c.308G>C (MYOCOS) ENSP00000490048.1:p.Cys103Ser
ENST00000638471.1:c.154C>G (MYOC) ENSP00000491206.1:p.His52Asp
ENST00000037502.10:c.624C>G (MYOC) ENSP00000037502.5:p.Asp208Glu
ENST00000614688.1:c.624C>G (MYOC) ENSP00000478680.1:p.Asp208Glu
NM_000261.1:c.624C>G (MYOC) NP_000252.1:p.Asp208Glu
NM_000261.2:c.624C>G (MYOC) MANE Select NP_000252.1:p.Asp208Glu