Canonical Allele Identifier: CA119172

Linked Data

ClinVar Variation Id: 7949
dbSNP Id: rs74315329

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636338G>A , CM000663.2:g.171636338G>A GRCh38
NC_000001.10:g.171605478G>A , CM000663.1:g.171605478G>A GRCh37
NC_000001.9:g.169872101G>A NCBI36
NG_008859.1:g.21296C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1102C>T (MYOC) MANE Select ENSP00000037502.5:p.Gln368Ter
ENST00000637303.1:c.235-2292G>A (MYOCOS) ENSP00000490048.1:n.235-2292G>A
ENST00000638471.1:c.*440C>T (MYOC) ENSP00000491206.1:n.*440C>T
ENST00000037502.10:c.1102C>T (MYOC) ENSP00000037502.5:p.Gln368Ter
ENST00000614688.1:c.*66C>T (MYOC) ENSP00000478680.1:n.*66C>T
NM_000261.1:c.1102C>T (MYOC) NP_000252.1:p.Gln368Ter
NM_000261.2:c.1102C>T (MYOC) MANE Select NP_000252.1:p.Gln368Ter