Canonical Allele Identifier: CA2649106620
Gene: MYOC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652661G>A , CM000663.2:g.171652661G>A GRCh38
NC_000001.10:g.171621801G>A , CM000663.1:g.171621801G>A GRCh37
NC_000001.9:g.169888424G>A NCBI36
NG_008859.1:g.4973C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.-50C>T MANE Select ENSP00000037502.5:n.-50C>T
ENST00000037502.10:c.-50C>T ENSP00000037502.5:n.-50C>T
NM_000261.2:c.-50C>T MANE Select NP_000252.1:n.-50C>T