Linked Data
dbSNP Id:
rs1561708975
gnomAD v4:
5-148827584-T-C
MyVariant Identifiers:
chr5:g.148207147T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148827584T>C , CM000667.2:g.148827584T>C | GRCh38 |
| NC_000005.9:g.148207147T>C , CM000667.1:g.148207147T>C | GRCh37 |
| NC_000005.8:g.148187340T>C | NCBI36 |
| NG_016421.1:g.5992T>C | |
| NG_016421.2:g.5992T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305988.6:c.753T>C MANE Select | ENSP00000305372.4:p.Asp251= | |
| ENST00000305988.5:c.753T>C | ENSP00000305372.4:p.Asp251= | |
| NM_000024.5:c.753T>C | NP_000015.1:p.Asp251= | |
| NM_000024.6:c.753T>C MANE Select | NP_000015.2:p.Asp251= |