Canonical Allele Identifier: CA343727104

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171638702T>A , CM000663.2:g.171638702T>A GRCh38
NC_000001.10:g.171607842T>A , CM000663.1:g.171607842T>A GRCh37
NC_000001.9:g.169874465T>A NCBI36
NG_008859.1:g.18932A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.625A>T (MYOC) MANE Select ENSP00000037502.5:p.Thr209Ser
ENST00000637303.1:c.307T>A (MYOCOS) ENSP00000490048.1:p.Cys103Ser
ENST00000638471.1:c.155A>T (MYOC) ENSP00000491206.1:p.His52Leu
ENST00000037502.10:c.625A>T (MYOC) ENSP00000037502.5:p.Thr209Ser
ENST00000614688.1:c.625A>T (MYOC) ENSP00000478680.1:p.Thr209Ser
NM_000261.1:c.625A>T (MYOC) NP_000252.1:p.Thr209Ser
NM_000261.2:c.625A>T (MYOC) MANE Select NP_000252.1:p.Thr209Ser