Canonical Allele Identifier: CA343723601

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636083A>G , CM000663.2:g.171636083A>G GRCh38
NC_000001.10:g.171605223A>G , CM000663.1:g.171605223A>G GRCh37
NC_000001.9:g.169871846A>G NCBI36
NG_008859.1:g.21551T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1357T>C (MYOC) MANE Select ENSP00000037502.5:p.Tyr453His
ENST00000637303.1:c.235-2547A>G (MYOCOS) ENSP00000490048.1:n.235-2547A>G
ENST00000638471.1:c.*695T>C (MYOC) ENSP00000491206.1:n.*695T>C
ENST00000037502.10:c.1357T>C (MYOC) ENSP00000037502.5:p.Tyr453His
ENST00000614688.1:c.*321T>C (MYOC) ENSP00000478680.1:n.*321T>C
NM_000261.1:c.1357T>C (MYOC) NP_000252.1:p.Tyr453His
NM_000261.2:c.1357T>C (MYOC) MANE Select NP_000252.1:p.Tyr453His