Linked Data
dbSNP Id:
rs376887908
ExAC:
16:2161623 G / A
gnomAD v2:
16-2161623-G-A
gnomAD v3:
16-2111622-G-A
gnomAD v4:
16-2111622-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2111622G>A , CM000678.2:g.2111622G>A | GRCh38 |
| NC_000016.9:g.2161623G>A , CM000678.1:g.2161623G>A | GRCh37 |
| NC_000016.8:g.2101624G>A | NCBI36 |
| NG_008617.1:g.29277C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262304.9:c.3545C>T MANE Select | ENSP00000262304.4:p.Ala1182Val | |
| ENST00000262304.8:c.3545C>T | ENSP00000262304.4:p.Ala1182Val | |
| ENST00000415938.7:n.310+718C>T | ||
| ENST00000423118.5:c.3545C>T | ENSP00000399501.1:p.Ala1182Val | |
| ENST00000468674.5:n.430+718C>T | ||
| ENST00000469241.2:n.495C>T | ||
| ENST00000483024.1:c.233+194C>T | ||
| ENST00000483731.5:n.790+718C>T | ||
| ENST00000488185.2:c.473-3264C>T | ||
| ENST00000565639.6:n.773+718C>T | ||
| ENST00000568591.5:c.2226+718C>T | ENSP00000457162.1:n.2226+718C>T | |
| ENST00000569983.5:n.421+718C>T | ||
| NM_000296.3:c.3545C>T | NP_000287.3:p.Ala1182Val | |
| NM_001009944.2:c.3545C>T | NP_001009944.2:p.Ala1182Val | |
| XM_005255370.2:c.500C>T | XP_005255427.1:p.Ala167Val | |
| XM_011522525.1:c.3623C>T | XP_011520827.1:p.Ala1208Val | |
| XM_011522526.1:c.3623C>T | XP_011520828.1:p.Ala1208Val | |
| XM_011522527.1:c.3623C>T | XP_011520829.1:p.Ala1208Val | |
| XM_011522528.1:c.3599C>T | XP_011520830.1:p.Ala1200Val | |
| XM_011522529.1:c.3599C>T | XP_011520831.1:p.Ala1200Val | |
| XM_011522530.1:c.3569C>T | XP_011520832.1:p.Ala1190Val | |
| XM_011522531.1:c.3551C>T | XP_011520833.1:p.Ala1184Val | |
| XM_011522532.1:c.3497C>T | XP_011520834.1:p.Ala1166Val | |
| XM_011522533.1:c.3416C>T | XP_011520835.1:p.Ala1139Val | |
| XM_011522534.1:c.3359C>T | XP_011520836.1:p.Ala1120Val | |
| XM_011522535.1:c.1445C>T | XP_011520837.1:p.Ala482Val | |
| XM_011522536.1:c.3623C>T | XP_011520838.1:p.Ala1208Val | |
| XM_011522537.1:c.623C>T | XP_011520839.1:p.Ala208Val | |
| XR_932867.1:n.3638C>T | ||
| XR_932868.1:n.3638C>T | ||
| XR_932869.1:n.3638C>T | ||
| XR_932870.1:n.3638C>T | ||
| XM_005255370.3:c.500C>T | XP_005255427.1:p.Ala167Val | |
| XM_011522528.3:c.3599C>T | XP_011520830.1:p.Ala1200Val | |
| XM_011522529.2:c.3599C>T | XP_011520831.1:p.Ala1200Val | |
| XM_011522537.2:c.623C>T | XP_011520839.1:p.Ala208Val | |
| XM_024450298.1:c.3665C>T | XP_024306066.1:p.Ala1222Val | |
| XM_024450299.1:c.3593C>T | XP_024306067.1:p.Ala1198Val | |
| XM_024450300.1:c.3455C>T | XP_024306068.1:p.Ala1152Val | |
| XM_024450301.1:c.1541C>T | XP_024306069.1:p.Ala514Val | |
| NM_000296.4:c.3545C>T | NP_000287.4:p.Ala1182Val | |
| NM_001009944.3:c.3545C>T MANE Select | NP_001009944.3:p.Ala1182Val |