Linked Data
ClinVar Variation Id:
618376
dbSNP Id:
rs767649515
gnomAD v3:
15-67187414-C-T
gnomAD v4:
15-67187414-C-T
MyVariant Identifiers:
chr15:g.67479752C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.67187414C>T , CM000677.2:g.67187414C>T | GRCh38 |
| NC_000015.9:g.67479752C>T , CM000677.1:g.67479752C>T | GRCh37 |
| NC_000015.8:g.65266806C>T | NCBI36 |
| NG_011990.1:g.126558C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000558428.6:c.474C>T | ENSP00000454165.2:p.Ala158= | |
| ENST00000558739.2:c.744C>T | ENSP00000453684.2:p.Ala248= | |
| ENST00000558827.2:c.474C>T | ENSP00000452767.2:p.Ala158= | |
| ENST00000559460.6:c.744C>T | ENSP00000453082.2:p.Ala248= | |
| ENST00000560424.2:c.1170C>T | ENSP00000455540.2:p.Ala390= | |
| ENST00000327367.9:c.1059C>T MANE Select | ENSP00000332973.4:p.Ala353= | |
| ENST00000679624.1:c.744C>T | ENSP00000505445.1:p.Ala248= | |
| ENST00000680689.1:n.762C>T | ||
| ENST00000681239.1:c.744C>T | ENSP00000505641.1:p.Ala248= | |
| ENST00000327367.8:c.1059C>T | ENSP00000332973.4:p.Ala353= | |
| ENST00000439724.7:c.927C>T | ENSP00000401133.3:p.Ala309= | |
| ENST00000537194.6:c.474C>T | ENSP00000445348.2:p.Ala158= | |
| ENST00000540846.6:c.744C>T | ENSP00000437757.2:p.Ala248= | |
| ENST00000558763.1:n.753C>T | ||
| ENST00000558894.5:c.606C>T | ENSP00000458060.1:p.Ala202= | |
| ENST00000560402.1:n.283-5459C>T | ||
| ENST00000560424.1:c.251C>T | ||
| NM_001145102.1:c.744C>T | NP_001138574.1:p.Ala248= | |
| NM_001145103.1:c.927C>T | NP_001138575.1:p.Ala309= | |
| NM_001145104.1:c.474C>T | NP_001138576.1:p.Ala158= | |
| NM_005902.3:c.1059C>T | NP_005893.1:p.Ala353= | |
| XM_011521559.1:c.927C>T | XP_011519861.1:p.Ala309= | |
| XM_011521560.1:c.912C>T | XP_011519862.1:p.Ala304= | |
| XM_011521559.3:c.927C>T | XP_011519861.1:p.Ala309= | |
| NM_005902.4:c.1059C>T MANE Select | NP_005893.1:p.Ala353= | |
| NM_001145102.2:c.744C>T | NP_001138574.1:p.Ala248= | |
| NM_001145103.2:c.927C>T | NP_001138575.1:p.Ala309= | |
| NM_001145104.2:c.474C>T | NP_001138576.1:p.Ala158= |