Canonical Allele Identifier: CA343724639

Linked Data

ClinVar Variation Id: 2498113
ClinVar RCV Id: RCV003219174

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636319C>A , CM000663.2:g.171636319C>A GRCh38
NC_000001.10:g.171605459C>A , CM000663.1:g.171605459C>A GRCh37
NC_000001.9:g.169872082C>A NCBI36
NG_008859.1:g.21315G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1121G>T (MYOC) MANE Select ENSP00000037502.5:p.Gly374Val
ENST00000637303.1:c.235-2311C>A (MYOCOS) ENSP00000490048.1:n.235-2311C>A
ENST00000638471.1:c.*459G>T (MYOC) ENSP00000491206.1:n.*459G>T
ENST00000037502.10:c.1121G>T (MYOC) ENSP00000037502.5:p.Gly374Val
ENST00000614688.1:c.*85G>T (MYOC) ENSP00000478680.1:n.*85G>T
NM_000261.1:c.1121G>T (MYOC) NP_000252.1:p.Gly374Val
NM_000261.2:c.1121G>T (MYOC) MANE Select NP_000252.1:p.Gly374Val