Canonical Allele Identifier: CA421938470
Gene: MYOC HGNC NCBI
MYOCOS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.171605386T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636246T>C , CM000663.2:g.171636246T>C GRCh38
NC_000001.10:g.171605386T>C , CM000663.1:g.171605386T>C GRCh37
NC_000001.9:g.169872009T>C NCBI36
NG_008859.1:g.21388A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1194A>G (MYOC) MANE Select ENSP00000037502.5:p.Lys398=
ENST00000637303.1:c.235-2384T>C (MYOCOS) ENSP00000490048.1:n.235-2384T>C
ENST00000638471.1:c.*532A>G (MYOC) ENSP00000491206.1:n.*532A>G
ENST00000037502.10:c.1194A>G (MYOC) ENSP00000037502.5:p.Lys398=
ENST00000614688.1:c.*158A>G (MYOC) ENSP00000478680.1:n.*158A>G
NM_000261.1:c.1194A>G (MYOC) NP_000252.1:p.Lys398=
NM_000261.2:c.1194A>G (MYOC) MANE Select NP_000252.1:p.Lys398=
Search 100 bp 5'
Search 100 bp 3'