Canonical Allele Identifier: CA421938646

Linked Data

MyVariant Identifiers: chr1:g.171605215T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636075T>A , CM000663.2:g.171636075T>A GRCh38
NC_000001.10:g.171605215T>A , CM000663.1:g.171605215T>A GRCh37
NC_000001.9:g.169871838T>A NCBI36
NG_008859.1:g.21559A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1365A>T (MYOC) MANE Select ENSP00000037502.5:p.Thr455=
ENST00000637303.1:c.235-2555T>A (MYOCOS) ENSP00000490048.1:n.235-2555T>A
ENST00000638471.1:c.*703A>T (MYOC) ENSP00000491206.1:n.*703A>T
ENST00000037502.10:c.1365A>T (MYOC) ENSP00000037502.5:p.Thr455=
ENST00000614688.1:c.*329A>T (MYOC) ENSP00000478680.1:n.*329A>T
NM_000261.1:c.1365A>T (MYOC) NP_000252.1:p.Thr455=
NM_000261.2:c.1365A>T (MYOC) MANE Select NP_000252.1:p.Thr455=