Linked Data
dbSNP Id:
rs749259873
ExAC:
10:69955275 T / C
gnomAD v2:
10-69955275-T-C
gnomAD v4:
10-68195518-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.68195518T>C , CM000672.2:g.68195518T>C | GRCh38 |
| NC_000010.10:g.69955275T>C , CM000672.1:g.69955275T>C | GRCh37 |
| NC_000010.9:g.69625281T>C | NCBI36 |
| NG_032118.1:g.94402T>C , LRG_410:g.94402T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354393.7:c.2319T>C | ENSP00000346369.2:p.Ala773= | |
| ENST00000540630.6:c.3198T>C | ENSP00000441668.3:p.Ala1066= | |
| ENST00000613327.5:c.3144T>C | ENSP00000480757.2:p.Ala1048= | |
| ENST00000688812.1:c.*407T>C | ENSP00000510658.1:n.*407T>C | |
| ENST00000690544.1:c.*2415T>C | ENSP00000508989.1:n.*2415T>C | |
| ENST00000358913.10:c.3144T>C MANE Select | ENSP00000351790.5:p.Ala1048= | |
| ENST00000354393.6:c.2319T>C | ENSP00000346369.2:p.Ala773= | |
| ENST00000358913.9:c.3144T>C | ENSP00000351790.5:p.Ala1048= | |
| ENST00000540630.5:c.3144T>C | ENSP00000441668.2:p.Ala1048= | |
| ENST00000613327.4:c.2262T>C | ENSP00000480757.1:p.Ala754= | |
| NM_001256267.1:c.3144T>C | NP_001243196.1:p.Ala1048= | |
| NM_001256268.1:c.2262T>C | NP_001243197.1:p.Ala754= | |
| NM_032578.3:c.3144T>C , LRG_410t1:c.3144T>C | NP_115967.2:p.Ala1048= | |
| NR_045662.3:n.2571T>C | ||
| NR_045663.3:n.3273T>C | ||
| XM_006718043.2:c.3198T>C | XP_006718106.1:p.Ala1066= | |
| XM_011540292.1:c.3174T>C | XP_011538594.1:p.Ala1058= | |
| XM_017016833.1:c.3222T>C | XP_016872322.1:p.Ala1074= | |
| XM_017016834.2:c.3144T>C | XP_016872323.1:p.Ala1048= | |
| XM_024448236.1:c.2022T>C | XP_024304004.1:p.Ala674= | |
| NR_045662.4:n.2681T>C | ||
| NR_045663.4:n.3218T>C | ||
| NM_001256267.2:c.3144T>C | NP_001243196.1:p.Ala1048= | |
| NM_001256268.2:c.2262T>C | NP_001243197.1:p.Ala754= | |
| NM_032578.4:c.3144T>C MANE Select | NP_115967.2:p.Ala1048= |