Canonical Allele Identifier: CA343718729
Gene: MYOC HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.171621434C>G (hg19) chr1:g.171652294C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652294C>G , CM000663.2:g.171652294C>G GRCh38
NC_000001.10:g.171621434C>G , CM000663.1:g.171621434C>G GRCh37
NC_000001.9:g.169888057C>G NCBI36
NG_008859.1:g.5340G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.318G>C MANE Select ENSP00000037502.5:p.Gln106His
ENST00000638471.1:c.130+188G>C ENSP00000491206.1:n.130+188G>C
ENST00000037502.10:c.318G>C ENSP00000037502.5:p.Gln106His
ENST00000614688.1:c.318G>C ENSP00000478680.1:p.Gln106His
NM_000261.1:c.318G>C NP_000252.1:p.Gln106His
NM_000261.2:c.318G>C MANE Select NP_000252.1:p.Gln106His
Search 100 bp 5'
Search 100 bp 3'