Linked Data
dbSNP Id:
rs2147088980
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.64192151T>A , CM000685.2:g.64192151T>A | GRCh38 |
| NC_000023.10:g.63412031T>A , CM000685.1:g.63412031T>A | GRCh37 |
| NC_000023.9:g.63328756T>A | NCBI36 |
| NG_021345.1:g.18594A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374869.8:c.1136A>T MANE Select | ENSP00000364003.4:p.Asp379Val | |
| ENST00000330258.3:c.1136A>T | ENSP00000329117.3:p.Asp379Val | |
| ENST00000374869.7:c.1136A>T | ENSP00000364003.3:p.Asp379Val | |
| NM_152424.3:c.1136A>T | NP_689637.3:p.Asp379Val | |
| XM_011530858.1:c.1136A>T | XP_011529160.1:p.Asp379Val | |
| NM_152424.4:c.1136A>T MANE Select | NP_689637.3:p.Asp379Val |