Linked Data
ClinVar Variation Id:
56454
ClinVar RCV Id:
RCV000049867
dbSNP Id:
rs386833896
gnomAD v4:
19-35845393-G-A
COSMIC:
COSM995258
PubMed:
PMID:11854170
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35845393G>A , CM000681.2:g.35845393G>A | GRCh38 |
| NC_000019.9:g.36336295G>A , CM000681.1:g.36336295G>A | GRCh37 |
| NC_000019.8:g.41028135G>A | NCBI36 |
| NG_013356.2:g.28895C>T , LRG_693:g.28895C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378910.10:c.1905C>T MANE Select | ENSP00000368190.4:p.Ser635= | |
| ENST00000353632.6:c.1905C>T | ENSP00000343634.5:p.Ser635= | |
| ENST00000378910.9:c.1905C>T | ENSP00000368190.4:p.Ser635= | |
| ENST00000585400.1:n.112+6C>T | ||
| NM_004646.3:c.1905C>T , LRG_693t1:c.1905C>T | NP_004637.1:p.Ser635= | |
| NM_004646.4:c.1905C>T MANE Select | NP_004637.1:p.Ser635= |