Linked Data
MyVariant Identifiers:
chr1:g.171605584C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171636444C>A , CM000663.2:g.171636444C>A | GRCh38 |
| NC_000001.10:g.171605584C>A , CM000663.1:g.171605584C>A | GRCh37 |
| NC_000001.9:g.169872207C>A | NCBI36 |
| NG_008859.1:g.21190G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.996G>T (MYOC) MANE Select | ENSP00000037502.5:p.Gly332= | |
| ENST00000637303.1:c.235-2186C>A (MYOCOS) | ENSP00000490048.1:n.235-2186C>A | |
| ENST00000638471.1:c.*334G>T (MYOC) | ENSP00000491206.1:n.*334G>T | |
| ENST00000037502.10:c.996G>T (MYOC) | ENSP00000037502.5:p.Gly332= | |
| ENST00000614688.1:c.996G>T (MYOC) | ENSP00000478680.1:p.Gly332= | |
| NM_000261.1:c.996G>T (MYOC) | NP_000252.1:p.Gly332= | |
| NM_000261.2:c.996G>T (MYOC) MANE Select | NP_000252.1:p.Gly332= |