Linked Data
ClinVar Variation Id:
17762
dbSNP Id:
rs56361140
gnomAD v4:
17-44260441-G-A
PubMed:
PMID:8704215
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44260441G>A , CM000679.2:g.44260441G>A | GRCh38 |
| NC_000017.10:g.42337809G>A , CM000679.1:g.42337809G>A | GRCh37 |
| NC_000017.9:g.39693335G>A | NCBI36 |
| NG_007498.1:g.12694C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262418.12:c.448C>T MANE Select | ENSP00000262418.6:p.Arg150Ter | |
| ENST00000262418.10:c.448C>T | ENSP00000262418.6:p.Arg150Ter | |
| ENST00000399246.3:c.448C>T | ENSP00000382190.3:p.Arg150Ter | |
| ENST00000471005.5:n.382C>T | ||
| ENST00000497360.5:n.587C>T | ||
| NM_000342.3:c.448C>T | NP_000333.1:p.Arg150Ter | |
| XM_005257593.3:c.253C>T | XP_005257650.1:p.Arg85Ter | |
| XM_011525129.1:c.448C>T | XP_011523431.1:p.Arg150Ter | |
| XM_011525130.1:c.448C>T | XP_011523432.1:p.Arg150Ter | |
| XM_011525131.1:c.448C>T | XP_011523433.1:p.Arg150Ter | |
| XM_005257593.5:c.253C>T | XP_005257650.1:p.Arg85Ter | |
| XM_011525129.2:c.448C>T | XP_011523431.1:p.Arg150Ter | |
| NM_000342.4:c.448C>T MANE Select | NP_000333.1:p.Arg150Ter |