Linked Data
dbSNP Id:
rs778893487
ExAC:
7:95818656 G / A
gnomAD v2:
7-95818656-G-A
gnomAD v4:
7-96189344-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.96189344G>A , CM000669.2:g.96189344G>A | GRCh38 |
| NC_000007.13:g.95818656G>A , CM000669.1:g.95818656G>A | GRCh37 |
| NC_000007.12:g.95656592G>A | NCBI36 |
| NG_012247.1:g.137804C>T | |
| NG_012247.2:g.137804C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265631.10:c.883C>T MANE Select | ENSP00000265631.6:p.Pro295Ser | |
| ENST00000265631.9:c.883C>T | ENSP00000265631.5:p.Pro295Ser | |
| ENST00000416240.6:c.883C>T | ENSP00000400101.2:p.Pro295Ser | |
| ENST00000484495.5:n.36C>T | ||
| NM_001160210.1:c.883C>T | NP_001153682.1:p.Pro295Ser | |
| NM_014251.2:c.883C>T | NP_055066.1:p.Pro295Ser | |
| NR_027662.1:n.958C>T | ||
| XM_006715831.2:c.916C>T | XP_006715894.1:p.Pro306Ser | |
| XM_011515727.1:c.916C>T | XP_011514029.1:p.Pro306Ser | |
| XM_011515728.1:c.31C>T | XP_011514030.1:p.Pro11Ser | |
| XM_006715831.4:c.916C>T | XP_006715894.1:p.Pro306Ser | |
| XM_011515727.3:c.916C>T | XP_011514029.1:p.Pro306Ser | |
| XM_017011663.1:c.874C>T | XP_016867152.1:p.Pro292Ser | |
| XM_017011664.2:c.31C>T | XP_016867153.1:p.Pro11Ser | |
| XM_017011665.1:c.31C>T | XP_016867154.1:p.Pro11Ser | |
| XR_001744525.2:n.1054C>T | ||
| XR_002956405.1:n.1196C>T | ||
| NM_014251.3:c.883C>T MANE Select | NP_055066.1:p.Pro295Ser | |
| NR_027662.2:n.909C>T | ||
| NM_001160210.2:c.883C>T | NP_001153682.1:p.Pro295Ser |