Canonical Allele Identifier: CA343723323

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636029A>C , CM000663.2:g.171636029A>C GRCh38
NC_000001.10:g.171605169A>C , CM000663.1:g.171605169A>C GRCh37
NC_000001.9:g.169871792A>C NCBI36
NG_008859.1:g.21605T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1411T>G (MYOC) MANE Select ENSP00000037502.5:p.Tyr471Asp
ENST00000637303.1:c.235-2601A>C (MYOCOS) ENSP00000490048.1:n.235-2601A>C
ENST00000638471.1:c.*749T>G (MYOC) ENSP00000491206.1:n.*749T>G
ENST00000037502.10:c.1411T>G (MYOC) ENSP00000037502.5:p.Tyr471Asp
ENST00000614688.1:c.*375T>G (MYOC) ENSP00000478680.1:n.*375T>G
NM_000261.1:c.1411T>G (MYOC) NP_000252.1:p.Tyr471Asp
NM_000261.2:c.1411T>G (MYOC) MANE Select NP_000252.1:p.Tyr471Asp