Linked Data
dbSNP Id:
rs1475557145
gnomAD v2:
10-112572176-A-C
gnomAD v3:
10-110812418-A-C
gnomAD v4:
10-110812418-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110812418A>C , CM000672.2:g.110812418A>C | GRCh38 |
| NC_000010.10:g.112572176A>C , CM000672.1:g.112572176A>C | GRCh37 |
| NC_000010.9:g.112562166A>C | NCBI36 |
| NG_021177.1:g.173022A>C , LRG_382:g.173022A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369519.4:c.2021A>C MANE Select | ENSP00000358532.3:p.Asp674Ala | |
| ENST00000369519.3:c.2021A>C | ENSP00000358532.3:p.Asp674Ala | |
| NM_001134363.2:c.2021A>C | NP_001127835.2:p.Asp674Ala | |
| XM_011539697.1:c.1637A>C | XP_011537999.1:p.Asp546Ala | |
| XM_017016103.2:c.1856A>C | XP_016871592.1:p.Asp619Ala | |
| XM_017016104.2:c.1637A>C | XP_016871593.1:p.Asp546Ala | |
| NM_001134363.3:c.2021A>C MANE Select | NP_001127835.2:p.Asp674Ala |