Canonical Allele Identifier: CA343723911

Linked Data

dbSNP Id: rs1367941231

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636139C>G , CM000663.2:g.171636139C>G GRCh38
NC_000001.10:g.171605279C>G , CM000663.1:g.171605279C>G GRCh37
NC_000001.9:g.169871902C>G NCBI36
NG_008859.1:g.21495G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1301G>C (MYOC) MANE Select ENSP00000037502.5:p.Gly434Ala
ENST00000637303.1:c.235-2491C>G (MYOCOS) ENSP00000490048.1:n.235-2491C>G
ENST00000638471.1:c.*639G>C (MYOC) ENSP00000491206.1:n.*639G>C
ENST00000037502.10:c.1301G>C (MYOC) ENSP00000037502.5:p.Gly434Ala
ENST00000614688.1:c.*265G>C (MYOC) ENSP00000478680.1:n.*265G>C
NM_000261.1:c.1301G>C (MYOC) NP_000252.1:p.Gly434Ala
NM_000261.2:c.1301G>C (MYOC) MANE Select NP_000252.1:p.Gly434Ala