Canonical Allele Identifier: CA32685813

Linked Data

dbSNP Id: rs909669034

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636436T>A , CM000663.2:g.171636436T>A GRCh38
NC_000001.10:g.171605576T>A , CM000663.1:g.171605576T>A GRCh37
NC_000001.9:g.169872199T>A NCBI36
NG_008859.1:g.21198A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1004A>T (MYOC) MANE Select ENSP00000037502.5:p.Tyr335Phe
ENST00000637303.1:c.235-2194T>A (MYOCOS) ENSP00000490048.1:n.235-2194T>A
ENST00000638471.1:c.*342A>T (MYOC) ENSP00000491206.1:n.*342A>T
ENST00000037502.10:c.1004A>T (MYOC) ENSP00000037502.5:p.Tyr335Phe
ENST00000614688.1:c.1004A>T (MYOC) ENSP00000478680.1:p.Tyr335Phe
NM_000261.1:c.1004A>T (MYOC) NP_000252.1:p.Tyr335Phe
NM_000261.2:c.1004A>T (MYOC) MANE Select NP_000252.1:p.Tyr335Phe