Canonical Allele Identifier: CA2843531602
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652630C>A , CM000663.2:g.171652630C>A GRCh38
NC_000001.10:g.171621770C>A , CM000663.1:g.171621770C>A GRCh37
NC_000001.9:g.169888393C>A NCBI36
NG_008859.1:g.5004G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.-19G>T MANE Select ENSP00000037502.5:n.-19G>T
ENST00000037502.10:c.-19G>T ENSP00000037502.5:n.-19G>T
ENST00000614688.1:c.-19G>T ENSP00000478680.1:n.-19G>T
NM_000261.1:c.-19G>T NP_000252.1:n.-19G>T
NM_000261.2:c.-19G>T MANE Select NP_000252.1:n.-19G>T