Linked Data
dbSNP Id:
rs372642553
ExAC:
16:2161557 G / T
gnomAD v2:
16-2161557-G-T
gnomAD v3:
16-2111556-G-T
gnomAD v4:
16-2111556-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2111556G>T , CM000678.2:g.2111556G>T | GRCh38 |
| NC_000016.9:g.2161557G>T , CM000678.1:g.2161557G>T | GRCh37 |
| NC_000016.8:g.2101558G>T | NCBI36 |
| NG_008617.1:g.29343C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262304.9:c.3611C>A MANE Select | ENSP00000262304.4:p.Ala1204Glu | |
| ENST00000262304.8:c.3611C>A | ENSP00000262304.4:p.Ala1204Glu | |
| ENST00000415938.7:n.310+784C>A | ||
| ENST00000423118.5:c.3611C>A | ENSP00000399501.1:p.Ala1204Glu | |
| ENST00000468674.5:n.430+784C>A | ||
| ENST00000469241.2:n.561C>A | ||
| ENST00000483024.1:c.233+260C>A | ||
| ENST00000483731.5:n.790+784C>A | ||
| ENST00000488185.2:c.473-3198C>A | ||
| ENST00000565639.6:n.773+784C>A | ||
| ENST00000568591.5:c.2226+784C>A | ENSP00000457162.1:n.2226+784C>A | |
| ENST00000569983.5:n.421+784C>A | ||
| NM_000296.3:c.3611C>A | NP_000287.3:p.Ala1204Glu | |
| NM_001009944.2:c.3611C>A | NP_001009944.2:p.Ala1204Glu | |
| XM_005255370.2:c.566C>A | XP_005255427.1:p.Ala189Glu | |
| XM_011522525.1:c.3689C>A | XP_011520827.1:p.Ala1230Glu | |
| XM_011522526.1:c.3689C>A | XP_011520828.1:p.Ala1230Glu | |
| XM_011522527.1:c.3689C>A | XP_011520829.1:p.Ala1230Glu | |
| XM_011522528.1:c.3665C>A | XP_011520830.1:p.Ala1222Glu | |
| XM_011522529.1:c.3665C>A | XP_011520831.1:p.Ala1222Glu | |
| XM_011522530.1:c.3635C>A | XP_011520832.1:p.Ala1212Glu | |
| XM_011522531.1:c.3617C>A | XP_011520833.1:p.Ala1206Glu | |
| XM_011522532.1:c.3563C>A | XP_011520834.1:p.Ala1188Glu | |
| XM_011522533.1:c.3482C>A | XP_011520835.1:p.Ala1161Glu | |
| XM_011522534.1:c.3425C>A | XP_011520836.1:p.Ala1142Glu | |
| XM_011522535.1:c.1511C>A | XP_011520837.1:p.Ala504Glu | |
| XM_011522536.1:c.3689C>A | XP_011520838.1:p.Ala1230Glu | |
| XM_011522537.1:c.689C>A | XP_011520839.1:p.Ala230Glu | |
| XR_932867.1:n.3704C>A | ||
| XR_932868.1:n.3704C>A | ||
| XR_932869.1:n.3704C>A | ||
| XR_932870.1:n.3704C>A | ||
| XM_005255370.3:c.566C>A | XP_005255427.1:p.Ala189Glu | |
| XM_011522528.3:c.3665C>A | XP_011520830.1:p.Ala1222Glu | |
| XM_011522529.2:c.3665C>A | XP_011520831.1:p.Ala1222Glu | |
| XM_011522537.2:c.689C>A | XP_011520839.1:p.Ala230Glu | |
| XM_024450298.1:c.3731C>A | XP_024306066.1:p.Ala1244Glu | |
| XM_024450299.1:c.3659C>A | XP_024306067.1:p.Ala1220Glu | |
| XM_024450300.1:c.3521C>A | XP_024306068.1:p.Ala1174Glu | |
| XM_024450301.1:c.1607C>A | XP_024306069.1:p.Ala536Glu | |
| NM_000296.4:c.3611C>A | NP_000287.4:p.Ala1204Glu | |
| NM_001009944.3:c.3611C>A MANE Select | NP_001009944.3:p.Ala1204Glu |