Linked Data
MyVariant Identifiers:
chr13:g.48923092G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48348956G>T , CM000675.2:g.48348956G>T | GRCh38 |
| NC_000013.10:g.48923092G>T , CM000675.1:g.48923092G>T | GRCh37 |
| NC_000013.9:g.47821093G>T | NCBI36 |
| NG_009009.1:g.50210G>T , LRG_517:g.50210G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.540G>T MANE Select | ENSP00000267163.4:p.Ser180= | |
| ENST00000650461.1:c.540G>T | ENSP00000497193.1:p.Ser180= | |
| ENST00000267163.4:c.540G>T | ENSP00000267163.4:p.Ser180= | |
| ENST00000467505.5:c.138-11061G>T | ENSP00000434702.1:n.138-11061G>T | |
| ENST00000525036.1:n.702G>T | ||
| NM_000321.2:c.540G>T , LRG_517t1:c.540G>T | NP_000312.2:p.Ser180= | |
| XM_011535171.1:c.279G>T | XP_011533473.1:p.Ser93= | |
| XM_011535171.2:c.279G>T | XP_011533473.1:p.Ser93= | |
| NM_000321.3:c.540G>T MANE Select | NP_000312.2:p.Ser180= |