Linked Data
ClinVar Variation Id:
2785080
ClinVar RCV Id:
RCV003621834
dbSNP Id:
rs1557339910
gnomAD v2:
X-148582539-G-A
gnomAD v3:
X-149501008-G-A
gnomAD v4:
X-149501008-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.149501008G>A , CM000685.2:g.149501008G>A | GRCh38 |
| NC_000023.10:g.148582539G>A , CM000685.1:g.148582539G>A | GRCh37 |
| NC_000023.9:g.148390444G>A | NCBI36 |
| NG_011900.3:g.9327C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340855.11:c.448C>T MANE Select | ENSP00000339801.6:p.Pro150Ser | |
| ENST00000651111.1:c.-186C>T | ENSP00000498395.1:n.-186C>T | |
| ENST00000340855.10:c.448C>T | ENSP00000339801.6:p.Pro150Ser | |
| ENST00000370441.8:c.448C>T | ENSP00000359470.4:p.Pro150Ser | |
| ENST00000422081.6:c.-186C>T | ENSP00000477056.1:n.-186C>T | |
| ENST00000441880.1:n.114-13910C>T | ||
| ENST00000464251.5:c.374C>T | ENSP00000428980.1:n.374C>T | |
| ENST00000466323.5:c.448C>T | ENSP00000418264.1:p.Pro150Ser | |
| ENST00000490775.5:n.107C>T | ||
| ENST00000523759.5:n.562C>T | ||
| NM_000202.6:c.448C>T | NP_000193.1:p.Pro150Ser | |
| NM_001166550.2:c.178C>T | NP_001160022.1:p.Pro60Ser | |
| NM_006123.4:c.448C>T | NP_006114.1:p.Pro150Ser | |
| NR_104128.1:n.665C>T | ||
| NM_000202.7:c.448C>T | NP_000193.1:p.Pro150Ser | |
| NM_001166550.3:c.178C>T | NP_001160022.1:p.Pro60Ser | |
| NM_000202.8:c.448C>T MANE Select | NP_000193.1:p.Pro150Ser | |
| NM_001166550.4:c.178C>T | NP_001160022.1:p.Pro60Ser | |
| NM_006123.5:c.448C>T | NP_006114.1:p.Pro150Ser | |
| NR_104128.2:n.617C>T |