Linked Data
ClinVar Variation Id:
1056659
ClinVar RCV Id:
RCV001365525
dbSNP Id:
rs2105962314
gnomAD v4:
2-202467606-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202467606C>A , CM000664.2:g.202467606C>A | GRCh38 |
| NC_000002.11:g.203332329C>A , CM000664.1:g.203332329C>A | GRCh37 |
| NC_000002.10:g.203040574C>A | NCBI36 |
| NG_009363.1:g.96280C>A , LRG_712:g.96280C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374580.10:c.335C>A MANE Select | ENSP00000363708.4:p.Thr112Lys | |
| ENST00000638587.1:c.266C>A | ENSP00000491062.1:p.Thr89Lys | |
| ENST00000374574.2:c.335C>A | ENSP00000363702.2:p.Thr112Lys | |
| ENST00000374580.8:c.335C>A | ENSP00000363708.4:p.Thr112Lys | |
| ENST00000479069.1:n.242C>A | ||
| NM_001204.6:c.335C>A , LRG_712t1:c.335C>A | NP_001195.2:p.Thr112Lys | |
| XM_011511687.1:c.335C>A | XP_011509989.1:p.Thr112Lys | |
| XM_011511688.1:c.335C>A | XP_011509990.1:p.Thr112Lys | |
| NM_001204.7:c.335C>A MANE Select | NP_001195.2:p.Thr112Lys |