Linked Data
MyVariant Identifiers:
chr22:g.44324754T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43928874T>C , CM000684.2:g.43928874T>C | GRCh38 |
| NC_000022.10:g.44324754T>C , CM000684.1:g.44324754T>C | GRCh37 |
| NC_000022.9:g.42656087T>C | NCBI36 |
| NG_008631.1:g.10136T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.471T>C MANE Select | ENSP00000216180.3:p.Pro157= | |
| ENST00000216180.7:c.471T>C | ENSP00000216180.3:p.Pro157= | |
| ENST00000406117.6:c.*103T>C | ENSP00000384668.2:n.*103T>C | |
| ENST00000423180.2:c.459T>C | ENSP00000397987.2:p.Pro153= | |
| ENST00000478713.1:n.505T>C | ||
| NM_025225.2:c.471T>C | NP_079501.2:p.Pro157= | |
| NM_025225.3:c.471T>C MANE Select | NP_079501.2:p.Pro157= |