Linked Data
ClinVar Variation Id:
1561510
ClinVar RCV Id:
RCV002211881
dbSNP Id:
rs891068141
gnomAD v4:
19-4816305-C-A
MyVariant Identifiers:
chr19:g.4816317C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816305C>A , CM000681.2:g.4816305C>A | GRCh38 |
| NC_000019.9:g.4816317C>A , CM000681.1:g.4816317C>A | GRCh37 |
| NC_000019.8:g.4767317C>A | NCBI36 |
| NG_031998.1:g.20438G>T , LRG_358:g.20438G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.2073G>T MANE Select | ENSP00000248244.4:p.Leu691= | |
| ENST00000248244.5:c.2073G>T | ENSP00000248244.4:p.Leu691= | |
| ENST00000621756.1:c.1575G>T | ENSP00000479467.1:p.Leu525= | |
| NM_182919.3:c.2073G>T , LRG_358t1:c.2073G>T | NP_891549.1:p.Leu691= | |
| NM_001385678.1:c.2031G>T | NP_001372607.1:p.Leu677= | |
| NM_001385679.1:c.1938G>T | NP_001372608.1:p.Leu646= | |
| NM_001385680.1:c.1431G>T | NP_001372609.1:p.Leu477= | |
| NM_182919.4:c.2073G>T MANE Select | NP_891549.1:p.Leu691= |