Linked Data
ClinVar Variation Id:
1137256
ClinVar RCV Id:
RCV001473161
dbSNP Id:
rs1315598449
COSMIC:
COSM5402682
MyVariant Identifiers:
chr5:g.149357530G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149977967G>A , CM000667.2:g.149977967G>A | GRCh38 |
| NC_000005.9:g.149357530G>A , CM000667.1:g.149357530G>A | GRCh37 |
| NC_000005.8:g.149337723G>A | NCBI36 |
| NG_007147.2:g.19085G>A , LRG_684:g.19085G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000690410.1:n.547G>A | ||
| ENST00000286298.5:c.315G>A MANE Select | ENSP00000286298.4:p.Lys105= | |
| ENST00000286298.4:c.315G>A | ENSP00000286298.4:p.Lys105= | |
| NM_000112.3:c.315G>A , LRG_684t1:c.315G>A | NP_000103.2:p.Lys105= | |
| XM_017009191.2:c.315G>A | XP_016864680.1:p.Lys105= | |
| NM_000112.4:c.315G>A MANE Select | NP_000103.2:p.Lys105= |