Linked Data
ClinVar Variation Id:
427153
ClinVar RCV Id:
RCV000489990
dbSNP Id:
rs1085307989
gnomAD v4:
7-143331583-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.143331583T>C , CM000669.2:g.143331583T>C | GRCh38 |
| NC_000007.13:g.143028676T>C , CM000669.1:g.143028676T>C | GRCh37 |
| NC_000007.12:g.142738798T>C | NCBI36 |
| NG_009815.1:g.20458T>C | |
| NG_009815.2:g.20458T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000650516.2:c.1097T>C | ENSP00000498052.2:p.Val366Ala | |
| ENST00000343257.7:c.1097T>C MANE Select | ENSP00000339867.2:p.Val366Ala | |
| ENST00000432192.6:c.921T>C | ||
| ENST00000343257.6:c.1097T>C | ENSP00000339867.2:p.Val366Ala | |
| NM_000083.2:c.1097T>C | NP_000074.2:p.Val366Ala | |
| NR_046453.1:n.1187T>C | ||
| XM_011515781.1:c.1097T>C | XP_011514083.1:p.Val366Ala | |
| XM_011515782.1:c.-73T>C | XP_011514084.1:n.-73T>C | |
| XM_011515782.2:c.-73T>C | XP_011514084.1:n.-73T>C | |
| XM_017011739.1:c.647T>C | XP_016867228.1:p.Val216Ala | |
| XM_017011740.1:c.647T>C | XP_016867229.1:p.Val216Ala | |
| NM_000083.3:c.1097T>C MANE Select | NP_000074.3:p.Val366Ala | |
| NR_046453.2:n.1202T>C |