Linked Data
MyVariant Identifiers:
chr1:g.119964520C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119421897C>A , CM000663.2:g.119421897C>A | GRCh38 |
| NC_000001.10:g.119964520C>A , CM000663.1:g.119964520C>A | GRCh37 |
| NC_000001.9:g.119766043C>A | NCBI36 |
| NG_013349.1:g.11967C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369416.4:c.396C>A MANE Select | ENSP00000358424.3:p.Ser132= | |
| ENST00000369416.3:c.396C>A | ENSP00000358424.3:p.Ser132= | |
| ENST00000433745.5:c.396C>A | ENSP00000388292.1:p.Ser132= | |
| ENST00000448448.2:n.340C>A | ||
| ENST00000543831.5:c.396C>A | ENSP00000445122.1:p.Ser132= | |
| NM_000198.3:c.396C>A | NP_000189.1:p.Ser132= | |
| NM_001166120.1:c.396C>A | NP_001159592.1:p.Ser132= | |
| NM_000198.4:c.396C>A MANE Select | NP_000189.1:p.Ser132= | |
| NM_001166120.2:c.396C>A | NP_001159592.1:p.Ser132= |