Canonical Allele Identifier: CA343723939

Linked Data

ClinVar Variation Id: 2500839
ClinVar RCV Id: RCV003226024

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636142C>T , CM000663.2:g.171636142C>T GRCh38
NC_000001.10:g.171605282C>T , CM000663.1:g.171605282C>T GRCh37
NC_000001.9:g.169871905C>T NCBI36
NG_008859.1:g.21492G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1298G>A (MYOC) MANE Select ENSP00000037502.5:p.Cys433Tyr
ENST00000637303.1:c.235-2488C>T (MYOCOS) ENSP00000490048.1:n.235-2488C>T
ENST00000638471.1:c.*636G>A (MYOC) ENSP00000491206.1:n.*636G>A
ENST00000037502.10:c.1298G>A (MYOC) ENSP00000037502.5:p.Cys433Tyr
ENST00000614688.1:c.*262G>A (MYOC) ENSP00000478680.1:n.*262G>A
NM_000261.1:c.1298G>A (MYOC) NP_000252.1:p.Cys433Tyr
NM_000261.2:c.1298G>A (MYOC) MANE Select NP_000252.1:p.Cys433Tyr