Linked Data
dbSNP Id:
rs755436316
ExAC:
16:47730344 T / C
gnomAD v2:
16-47730344-T-C
gnomAD v3:
16-47696433-T-C
gnomAD v4:
16-47696433-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.47696433T>C , CM000678.2:g.47696433T>C | GRCh38 |
| NC_000016.9:g.47730344T>C , CM000678.1:g.47730344T>C | GRCh37 |
| NC_000016.8:g.46287845T>C | NCBI36 |
| NG_016598.1:g.240135T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696809.1:c.*1522T>C | ENSP00000512887.1:n.*1522T>C | |
| ENST00000699276.1:c.*576T>C | ENSP00000514257.1:n.*576T>C | |
| ENST00000323584.10:c.2948T>C MANE Select | ENSP00000313504.5:p.Val983Ala | |
| ENST00000299167.12:c.2948T>C | ENSP00000299167.8:p.Val983Ala | |
| ENST00000323584.9:c.2948T>C | ENSP00000313504.5:p.Val983Ala | |
| ENST00000566044.5:c.2927T>C | ENSP00000456729.1:p.Val976Ala | |
| ENST00000566319.2:n.1764T>C | ||
| NM_000293.2:c.2948T>C | NP_000284.1:p.Val983Ala | |
| NM_001031835.2:c.2927T>C | NP_001027005.1:p.Val976Ala | |
| XM_005255983.3:c.2948T>C | XP_005256040.1:p.Val983Ala | |
| XM_005255984.3:c.2927T>C | XP_005256041.1:p.Val976Ala | |
| XM_011523107.1:c.1526T>C | XP_011521409.1:p.Val509Ala | |
| NM_001363837.1:c.2948T>C | NP_001350766.1:p.Val983Ala | |
| XM_005255983.4:c.2948T>C | XP_005256040.1:p.Val983Ala | |
| XM_005255984.4:c.2927T>C | XP_005256041.1:p.Val976Ala | |
| XM_017023282.1:c.1835T>C | XP_016878771.1:p.Val612Ala | |
| XM_017023283.1:c.1526T>C | XP_016878772.1:p.Val509Ala | |
| XM_017023284.1:c.1526T>C | XP_016878773.1:p.Val509Ala | |
| XR_001751913.1:n.2872T>C | ||
| NM_000293.3:c.2948T>C MANE Select | NP_000284.1:p.Val983Ala | |
| NM_001031835.3:c.2927T>C | NP_001027005.1:p.Val976Ala |