Linked Data
dbSNP Id:
rs554233781
ExAC:
11:9225651 C / T
gnomAD v2:
11-9225651-C-T
gnomAD v3:
11-9204104-C-T
gnomAD v4:
11-9204104-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.9204104C>T , CM000673.2:g.9204104C>T | GRCh38 |
| NC_000011.9:g.9225651C>T , CM000673.1:g.9225651C>T | GRCh37 |
| NC_000011.8:g.9182227C>T | NCBI36 |
| NG_053019.1:g.66232G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328194.8:c.505G>A MANE Select | ENSP00000328524.3:p.Ala169Thr | |
| ENST00000530780.2:c.*331G>A | ENSP00000433925.1:n.*331G>A | |
| ENST00000530867.2:n.294G>A | ||
| ENST00000532696.2:n.428G>A | ||
| ENST00000679446.1:n.426G>A | ||
| ENST00000679460.1:n.294G>A | ||
| ENST00000679568.1:c.505G>A | ENSP00000505860.1:p.Ala169Thr | |
| ENST00000679745.1:n.294G>A | ||
| ENST00000679999.1:c.505G>A | ENSP00000505198.1:p.Ala169Thr | |
| ENST00000680252.1:c.294G>A | ||
| ENST00000680294.1:c.505G>A | ENSP00000506113.1:p.Ala169Thr | |
| ENST00000680470.1:c.505G>A | ENSP00000505975.1:p.Ala169Thr | |
| ENST00000680554.1:c.217G>A | ENSP00000505621.1:p.Ala73Thr | |
| ENST00000680576.1:n.294G>A | ||
| ENST00000680599.1:n.422G>A | ||
| ENST00000680742.1:c.505G>A | ENSP00000505206.1:p.Ala169Thr | |
| ENST00000680885.1:n.426G>A | ||
| ENST00000681158.1:c.294G>A | ||
| ENST00000681173.1:n.294G>A | ||
| ENST00000681203.1:c.433G>A | ENSP00000506456.1:p.Ala145Thr | |
| ENST00000681425.1:n.426G>A | ||
| ENST00000681915.1:n.294G>A | ||
| ENST00000328194.7:c.505G>A | ENSP00000328524.3:p.Ala169Thr | |
| ENST00000526707.5:c.433G>A | ENSP00000436780.1:p.Ala145Thr | |
| ENST00000530044.5:c.505G>A | ENSP00000435866.1:p.Ala169Thr | |
| ENST00000530780.1:c.*331G>A | ENSP00000433925.1:n.*331G>A | |
| ENST00000532696.1:n.260G>A | ||
| NM_001243254.1:c.505G>A | NP_001230183.1:p.Ala169Thr | |
| NM_015213.3:c.505G>A | NP_056028.2:p.Ala169Thr | |
| XM_005252832.1:c.505G>A | XP_005252889.1:p.Ala169Thr | |
| XM_011519952.1:c.505G>A | XP_011518254.1:p.Ala169Thr | |
| XR_242782.2:n.770G>A | ||
| XR_930851.1:n.770G>A | ||
| XR_930852.1:n.770G>A | ||
| XR_930853.1:n.770G>A | ||
| NM_001348749.1:c.433G>A | NP_001335678.1:p.Ala145Thr | |
| NM_001348750.1:c.217G>A | NP_001335679.1:p.Ala73Thr | |
| NR_145966.2:n.762G>A | ||
| NM_015213.4:c.505G>A MANE Select | NP_056028.2:p.Ala169Thr | |
| NM_001243254.2:c.505G>A | NP_001230183.1:p.Ala169Thr | |
| NM_001348749.2:c.433G>A | NP_001335678.1:p.Ala145Thr | |
| NM_001348750.2:c.217G>A | NP_001335679.1:p.Ala73Thr |