Linked Data
dbSNP Id:
rs546145028
gnomAD v2:
3-13896199-C-T
gnomAD v3:
3-13854702-C-T
gnomAD v4:
3-13854702-C-T
COSMIC:
COSM6028771
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.13854702C>T , CM000665.2:g.13854702C>T | GRCh38 |
| NC_000003.11:g.13896199C>T , CM000665.1:g.13896199C>T | GRCh37 |
| NC_000003.10:g.13871200C>T | NCBI36 |
| NG_008088.1:g.30420G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285018.5:c.400G>A MANE Select | ENSP00000285018.4:p.Asp134Asn | |
| ENST00000285018.4:c.400G>A | ENSP00000285018.4:p.Asp134Asn | |
| NM_004625.3:c.400G>A | NP_004616.2:p.Asp134Asn | |
| XM_011534090.1:c.199G>A | XP_011532392.1:p.Asp67Asn | |
| XM_011534091.1:c.199G>A | XP_011532393.1:p.Asp67Asn | |
| XM_011534091.2:c.199G>A | XP_011532393.1:p.Asp67Asn | |
| NM_004625.4:c.400G>A MANE Select | NP_004616.2:p.Asp134Asn |