Canonical Allele Identifier: CA421939234
Gene: MYOC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.171621683C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652543C>G , CM000663.2:g.171652543C>G GRCh38
NC_000001.10:g.171621683C>G , CM000663.1:g.171621683C>G GRCh37
NC_000001.9:g.169888306C>G NCBI36
NG_008859.1:g.5091G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.69G>C MANE Select ENSP00000037502.5:p.Leu23=
ENST00000638471.1:c.69G>C ENSP00000491206.1:p.Leu23=
ENST00000037502.10:c.69G>C ENSP00000037502.5:p.Leu23=
ENST00000614688.1:c.69G>C ENSP00000478680.1:p.Leu23=
NM_000261.1:c.69G>C NP_000252.1:p.Leu23=
NM_000261.2:c.69G>C MANE Select NP_000252.1:p.Leu23=