Canonical Allele Identifier: CA2649106628
Gene: MYOC HGNC NCBI

Linked Data

gnomAD v4: 1-171652672-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652672G>T , CM000663.2:g.171652672G>T GRCh38
NC_000001.10:g.171621812G>T , CM000663.1:g.171621812G>T GRCh37
NC_000001.9:g.169888435G>T NCBI36
NG_008859.1:g.4962C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.-61C>A MANE Select ENSP00000037502.5:n.-61C>A
ENST00000037502.10:c.-61C>A ENSP00000037502.5:n.-61C>A
NM_000261.2:c.-61C>A MANE Select NP_000252.1:n.-61C>A
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