Canonical Allele Identifier: CA2649106615
Gene: MYOC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652654C>G , CM000663.2:g.171652654C>G GRCh38
NC_000001.10:g.171621794C>G , CM000663.1:g.171621794C>G GRCh37
NC_000001.9:g.169888417C>G NCBI36
NG_008859.1:g.4980G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.-43G>C MANE Select ENSP00000037502.5:n.-43G>C
ENST00000037502.10:c.-43G>C ENSP00000037502.5:n.-43G>C
NM_000261.2:c.-43G>C MANE Select NP_000252.1:n.-43G>C