Canonical Allele Identifier: CA32685343

Linked Data

dbSNP Id: rs760260934

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636013A>T , CM000663.2:g.171636013A>T GRCh38
NC_000001.10:g.171605153A>T , CM000663.1:g.171605153A>T GRCh37
NC_000001.9:g.169871776A>T NCBI36
NG_008859.1:g.21621T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1427T>A (MYOC) MANE Select ENSP00000037502.5:p.Met476Lys
ENST00000637303.1:c.235-2617A>T (MYOCOS) ENSP00000490048.1:n.235-2617A>T
ENST00000638471.1:c.*765T>A (MYOC) ENSP00000491206.1:n.*765T>A
ENST00000037502.10:c.1427T>A (MYOC) ENSP00000037502.5:p.Met476Lys
ENST00000614688.1:c.*391T>A (MYOC) ENSP00000478680.1:n.*391T>A
NM_000261.1:c.1427T>A (MYOC) NP_000252.1:p.Met476Lys
NM_000261.2:c.1427T>A (MYOC) MANE Select NP_000252.1:p.Met476Lys