Linked Data
ClinVar Variation Id:
10147
ClinVar RCV Id:
RCV000010860
dbSNP Id:
rs137852374
ExAC:
X:154065973 G / A
gnomAD v2:
X-154065973-G-A
gnomAD v4:
X-154837698-G-A
PubMed:
PMID:1908817
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154837698G>A , CM000685.2:g.154837698G>A | GRCh38 |
| NC_000023.10:g.154065973G>A , CM000685.1:g.154065973G>A | GRCh37 |
| NC_000023.9:g.153719167G>A | NCBI36 |
| NG_011403.1:g.190026C>T | |
| NG_033065.1:g.1965C>T | |
| NG_011403.2:g.190026C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.6955C>T MANE Select | ENSP00000353393.4:p.Pro2319Ser | |
| ENST00000644698.1:c.688C>T | ENSP00000495706.1:p.Pro230Ser | |
| ENST00000330287.10:c.550C>T | ENSP00000327895.6:p.Pro184Ser | |
| ENST00000360256.8:c.6955C>T | ENSP00000353393.4:p.Pro2319Ser | |
| NM_000132.3:c.6955C>T | NP_000123.1:p.Pro2319Ser | |
| NM_019863.2:c.550C>T | NP_063916.1:p.Pro184Ser | |
| XM_011531126.1:c.6850C>T | XP_011529428.1:p.Pro2284Ser | |
| NM_000132.4:c.6955C>T MANE Select | NP_000123.1:p.Pro2319Ser | |
| NM_019863.3:c.550C>T | NP_063916.1:p.Pro184Ser |