Linked Data
ClinVar Variation Id:
1769072
dbSNP Id:
rs754657555
ExAC:
7:117144381 T / C
gnomAD v2:
7-117144381-T-C
gnomAD v3:
7-117504327-T-C
gnomAD v4:
7-117504327-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117504327T>C , CM000669.2:g.117504327T>C | GRCh38 |
| NC_000007.13:g.117144381T>C , CM000669.1:g.117144381T>C | GRCh37 |
| NC_000007.12:g.116931617T>C | NCBI36 |
| NG_016465.4:g.43544T>C , LRG_663:g.43544T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647720.2:c.128T>C | ENSP00000497673.2:p.Val43Ala | |
| ENST00000647978.2:c.128T>C | ENSP00000497658.1:p.Val43Ala | |
| ENST00000649781.2:c.128T>C | ENSP00000497203.1:p.Val43Ala | |
| ENST00000649850.2:c.128T>C | ENSP00000514457.1:p.Val43Ala | |
| ENST00000685018.2:c.128T>C | ENSP00000510194.2:p.Val43Ala | |
| ENST00000687278.2:c.128T>C | ENSP00000509593.2:p.Val43Ala | |
| ENST00000693465.2:n.213T>C | ||
| ENST00000699585.1:c.128T>C | ENSP00000514456.1:p.Val43Ala | |
| ENST00000699596.1:c.128T>C | ENSP00000514465.1:p.Val43Ala | |
| ENST00000699597.1:c.128T>C | ENSP00000514466.1:p.Val43Ala | |
| ENST00000699598.1:c.128T>C | ENSP00000514467.1:p.Val43Ala | |
| ENST00000699599.1:c.128T>C | ENSP00000514468.1:p.Val43Ala | |
| ENST00000699600.1:c.128T>C | ENSP00000514469.1:p.Val43Ala | |
| ENST00000699601.1:c.128T>C | ENSP00000514470.1:p.Val43Ala | |
| ENST00000699602.1:c.128T>C | ENSP00000514471.1:p.Val43Ala | |
| ENST00000699604.1:c.128T>C | ENSP00000514472.1:p.Val43Ala | |
| ENST00000699605.1:c.-116T>C | ENSP00000514473.1:n.-116T>C | |
| ENST00000446805.2:c.-116T>C | ENSP00000417012.1:n.-116T>C | |
| ENST00000693465.1:n.198T>C | ||
| ENST00000003084.11:c.128T>C MANE Select | ENSP00000003084.6:p.Val43Ala | |
| ENST00000647639.1:n.212T>C | ||
| ENST00000647978.1:c.128T>C | ENSP00000497658.1:p.Val43Ala | |
| ENST00000648260.1:c.128T>C | ENSP00000497957.1:p.Val43Ala | |
| ENST00000649406.1:c.128T>C | ENSP00000497965.1:p.Val43Ala | |
| ENST00000649781.1:c.128T>C | ENSP00000497203.1:p.Val43Ala | |
| ENST00000649850.1:n.211T>C | ||
| ENST00000673785.1:c.-116T>C | ENSP00000501235.1:n.-116T>C | |
| ENST00000003084.10:c.128T>C | ENSP00000003084.6:p.Val43Ala | |
| ENST00000426809.5:c.128T>C | ENSP00000389119.1:p.Val43Ala | |
| ENST00000446805.1:c.-116T>C | ENSP00000417012.1:n.-116T>C | |
| NM_000492.3:c.128T>C , LRG_663t1:c.128T>C | NP_000483.3:p.Val43Ala | |
| XM_011515751.1:c.218T>C | XP_011514053.1:p.Val73Ala | |
| XM_011515752.1:c.218T>C | XP_011514054.1:p.Val73Ala | |
| XM_011515753.1:c.-116T>C | XP_011514055.1:n.-116T>C | |
| XM_011515754.1:c.-190T>C | XP_011514056.1:n.-190T>C | |
| NM_000492.4:c.128T>C MANE Select | NP_000483.3:p.Val43Ala |