Linked Data
MyVariant Identifiers:
chr13:g.48923134T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48348998T>G , CM000675.2:g.48348998T>G | GRCh38 |
| NC_000013.10:g.48923134T>G , CM000675.1:g.48923134T>G | GRCh37 |
| NC_000013.9:g.47821135T>G | NCBI36 |
| NG_009009.1:g.50252T>G , LRG_517:g.50252T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.582T>G MANE Select | ENSP00000267163.4:p.Ser194= | |
| ENST00000650461.1:c.582T>G | ENSP00000497193.1:p.Ser194= | |
| ENST00000267163.4:c.582T>G | ENSP00000267163.4:p.Ser194= | |
| ENST00000467505.5:c.138-11019T>G | ENSP00000434702.1:n.138-11019T>G | |
| ENST00000525036.1:n.744T>G | ||
| NM_000321.2:c.582T>G , LRG_517t1:c.582T>G | NP_000312.2:p.Ser194= | |
| XM_011535171.1:c.321T>G | XP_011533473.1:p.Ser107= | |
| XM_011535171.2:c.321T>G | XP_011533473.1:p.Ser107= | |
| NM_000321.3:c.582T>G MANE Select | NP_000312.2:p.Ser194= |