Linked Data
MyVariant Identifiers:
chr13:g.20763436C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20189297C>T , CM000675.2:g.20189297C>T | GRCh38 |
| NC_000013.10:g.20763436C>T , CM000675.1:g.20763436C>T | GRCh37 |
| NC_000013.9:g.19661436C>T | NCBI36 |
| NG_008358.1:g.8679G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000382844.2:c.285G>A | ENSP00000372295.1:p.Val95= | |
| ENST00000382848.5:c.285G>A MANE Select | ENSP00000372299.4:p.Val95= | |
| ENST00000382844.1:c.285G>A | ENSP00000372295.1:p.Val95= | |
| ENST00000382848.4:c.285G>A | ENSP00000372299.4:p.Val95= | |
| NM_004004.5:c.285G>A | NP_003995.2:p.Val95= | |
| XM_011535049.1:c.285G>A | XP_011533351.1:p.Val95= | |
| XM_011535049.2:c.285G>A | XP_011533351.1:p.Val95= | |
| NM_004004.6:c.285G>A MANE Select | NP_003995.2:p.Val95= |