Canonical Allele Identifier: CA891106046

Linked Data

dbSNP Id: rs1298679111

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635720A>G , CM000663.2:g.171635720A>G GRCh38
NC_000001.10:g.171604860A>G , CM000663.1:g.171604860A>G GRCh37
NC_000001.9:g.169871483A>G NCBI36
NG_008859.1:g.21914T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*205T>C (MYOC) MANE Select ENSP00000037502.5:n.*205T>C
ENST00000637303.1:c.235-2910A>G (MYOCOS) ENSP00000490048.1:n.235-2910A>G
ENST00000638471.1:c.*1058T>C (MYOC) ENSP00000491206.1:n.*1058T>C
ENST00000037502.10:c.*205T>C (MYOC) ENSP00000037502.5:n.*205T>C
ENST00000614688.1:c.*684T>C (MYOC) ENSP00000478680.1:n.*684T>C
NM_000261.1:c.*205T>C (MYOC) NP_000252.1:n.*205T>C
NM_000261.2:c.*205T>C (MYOC) MANE Select NP_000252.1:n.*205T>C