Canonical Allele Identifier: CA2649105851

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635646T>C , CM000663.2:g.171635646T>C GRCh38
NC_000001.10:g.171604786T>C , CM000663.1:g.171604786T>C GRCh37
NC_000001.9:g.169871409T>C NCBI36
NG_008859.1:g.21988A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.*279A>G (MYOC) MANE Select ENSP00000037502.5:n.*279A>G
ENST00000637303.1:c.235-2984T>C (MYOCOS) ENSP00000490048.1:n.235-2984T>C
ENST00000638471.1:c.*1132A>G (MYOC) ENSP00000491206.1:n.*1132A>G
ENST00000037502.10:c.*279A>G (MYOC) ENSP00000037502.5:n.*279A>G
ENST00000614688.1:c.*758A>G (MYOC) ENSP00000478680.1:n.*758A>G
NM_000261.1:c.*279A>G (MYOC) NP_000252.1:n.*279A>G
NM_000261.2:c.*279A>G (MYOC) MANE Select NP_000252.1:n.*279A>G