Canonical Allele Identifier: CA2649105990

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635923T>A , CM000663.2:g.171635923T>A GRCh38
NC_000001.10:g.171605063T>A , CM000663.1:g.171605063T>A GRCh37
NC_000001.9:g.169871686T>A NCBI36
NG_008859.1:g.21711A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*2A>T (MYOC) MANE Select ENSP00000037502.5:n.*2A>T
ENST00000637303.1:c.235-2707T>A (MYOCOS) ENSP00000490048.1:n.235-2707T>A
ENST00000638471.1:c.*855A>T (MYOC) ENSP00000491206.1:n.*855A>T
ENST00000037502.10:c.*2A>T (MYOC) ENSP00000037502.5:n.*2A>T
ENST00000614688.1:c.*481A>T (MYOC) ENSP00000478680.1:n.*481A>T
NM_000261.1:c.*2A>T (MYOC) NP_000252.1:n.*2A>T
NM_000261.2:c.*2A>T (MYOC) MANE Select NP_000252.1:n.*2A>T