Canonical Allele Identifier: CA2746628366
Gene: MYOC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652677C>G , CM000663.2:g.171652677C>G GRCh38
NC_000001.10:g.171621817C>G , CM000663.1:g.171621817C>G GRCh37
NC_000001.9:g.169888440C>G NCBI36
NG_008859.1:g.4957G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.-66G>C MANE Select ENSP00000037502.5:n.-66G>C
ENST00000037502.10:c.-66G>C ENSP00000037502.5:n.-66G>C
NM_000261.2:c.-66G>C MANE Select NP_000252.1:n.-66G>C