Canonical Allele Identifier: CA421938466

Linked Data

MyVariant Identifiers: chr1:g.171605380G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171636240G>T , CM000663.2:g.171636240G>T GRCh38
NC_000001.10:g.171605380G>T , CM000663.1:g.171605380G>T GRCh37
NC_000001.9:g.169872003G>T NCBI36
NG_008859.1:g.21394C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000037502.11:c.1200C>A (MYOC) MANE Select ENSP00000037502.5:p.Ala400=
ENST00000637303.1:c.235-2390G>T (MYOCOS) ENSP00000490048.1:n.235-2390G>T
ENST00000638471.1:c.*538C>A (MYOC) ENSP00000491206.1:n.*538C>A
ENST00000037502.10:c.1200C>A (MYOC) ENSP00000037502.5:p.Ala400=
ENST00000614688.1:c.*164C>A (MYOC) ENSP00000478680.1:n.*164C>A
NM_000261.1:c.1200C>A (MYOC) NP_000252.1:p.Ala400=
NM_000261.2:c.1200C>A (MYOC) MANE Select NP_000252.1:p.Ala400=