Canonical Allele Identifier: CA421938801

Linked Data

MyVariant Identifiers: chr1:g.171605362C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636222C>T , CM000663.2:g.171636222C>T GRCh38
NC_000001.10:g.171605362C>T , CM000663.1:g.171605362C>T GRCh37
NC_000001.9:g.169871985C>T NCBI36
NG_008859.1:g.21412G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000037502.11:c.1218G>A (MYOC) MANE Select ENSP00000037502.5:p.Leu406=
ENST00000637303.1:c.235-2408C>T (MYOCOS) ENSP00000490048.1:n.235-2408C>T
ENST00000638471.1:c.*556G>A (MYOC) ENSP00000491206.1:n.*556G>A
ENST00000037502.10:c.1218G>A (MYOC) ENSP00000037502.5:p.Leu406=
ENST00000614688.1:c.*182G>A (MYOC) ENSP00000478680.1:n.*182G>A
NM_000261.1:c.1218G>A (MYOC) NP_000252.1:p.Leu406=
NM_000261.2:c.1218G>A (MYOC) MANE Select NP_000252.1:p.Leu406=