Canonical Allele Identifier: CA343722951

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171635964C>G , CM000663.2:g.171635964C>G GRCh38
NC_000001.10:g.171605104C>G , CM000663.1:g.171605104C>G GRCh37
NC_000001.9:g.169871727C>G NCBI36
NG_008859.1:g.21670G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1476G>C (MYOC) MANE Select ENSP00000037502.5:p.Leu492Phe
ENST00000637303.1:c.235-2666C>G (MYOCOS) ENSP00000490048.1:n.235-2666C>G
ENST00000638471.1:c.*814G>C (MYOC) ENSP00000491206.1:n.*814G>C
ENST00000037502.10:c.1476G>C (MYOC) ENSP00000037502.5:p.Leu492Phe
ENST00000614688.1:c.*440G>C (MYOC) ENSP00000478680.1:n.*440G>C
NM_000261.1:c.1476G>C (MYOC) NP_000252.1:p.Leu492Phe
NM_000261.2:c.1476G>C (MYOC) MANE Select NP_000252.1:p.Leu492Phe