Linked Data
ClinVar Variation Id:
56490
dbSNP Id:
rs386833929
gnomAD v3:
19-35851373-G-C
gnomAD v4:
19-35851373-G-C
PubMed:
PMID:18614772
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.35851373G>C , CM000681.2:g.35851373G>C | GRCh38 |
| NC_000019.9:g.36342275G>C , CM000681.1:g.36342275G>C | GRCh37 |
| NC_000019.8:g.41034115G>C | NCBI36 |
| NG_013356.2:g.22915C>G , LRG_693:g.22915C>G | |
| NG_051206.1:g.4739G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378910.10:c.286C>G MANE Select | ENSP00000368190.4:p.Leu96Val | |
| ENST00000353632.6:c.286C>G | ENSP00000343634.5:p.Leu96Val | |
| ENST00000378910.9:c.286C>G | ENSP00000368190.4:p.Leu96Val | |
| NM_004646.3:c.286C>G , LRG_693t1:c.286C>G | NP_004637.1:p.Leu96Val | |
| NM_004646.4:c.286C>G MANE Select | NP_004637.1:p.Leu96Val |