Canonical Allele Identifier: CA1207023294
Gene: MYOC HGNC NCBI

Linked Data

dbSNP Id: rs1653383548

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171652647T>C , CM000663.2:g.171652647T>C GRCh38
NC_000001.10:g.171621787T>C , CM000663.1:g.171621787T>C GRCh37
NC_000001.9:g.169888410T>C NCBI36
NG_008859.1:g.4987A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.-36A>G MANE Select ENSP00000037502.5:n.-36A>G
ENST00000037502.10:c.-36A>G ENSP00000037502.5:n.-36A>G
NM_000261.2:c.-36A>G MANE Select NP_000252.1:n.-36A>G