Linked Data
ClinVar Variation Id:
2500831
ClinVar RCV Id:
RCV003226016
dbSNP Id:
rs2234929
ExAC:
1:171605116 G / A
gnomAD v2:
1-171605116-G-A
gnomAD v3:
1-171635976-G-A
gnomAD v4:
1-171635976-G-A
ERepo:
CA1244015/MONDO:0007665/019
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171635976G>A , CM000663.2:g.171635976G>A | GRCh38 |
| NC_000001.10:g.171605116G>A , CM000663.1:g.171605116G>A | GRCh37 |
| NC_000001.9:g.169871739G>A | NCBI36 |
| NG_008859.1:g.21658C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.1464C>T (MYOC) MANE Select | ENSP00000037502.5:p.Ala488= | |
| ENST00000637303.1:c.235-2654G>A (MYOCOS) | ENSP00000490048.1:n.235-2654G>A | |
| ENST00000638471.1:c.*802C>T (MYOC) | ENSP00000491206.1:n.*802C>T | |
| ENST00000037502.10:c.1464C>T (MYOC) | ENSP00000037502.5:p.Ala488= | |
| ENST00000614688.1:c.*428C>T (MYOC) | ENSP00000478680.1:n.*428C>T | |
| NM_000261.1:c.1464C>T (MYOC) | NP_000252.1:p.Ala488= | |
| NM_000261.2:c.1464C>T (MYOC) MANE Select | NP_000252.1:p.Ala488= |