Linked Data
dbSNP Id:
rs1244615706
gnomAD v2:
2-215845268-G-A
gnomAD v3:
2-214980544-G-A
gnomAD v4:
2-214980544-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214980544G>A , CM000664.2:g.214980544G>A | GRCh38 |
| NC_000002.11:g.215845268G>A , CM000664.1:g.215845268G>A | GRCh37 |
| NC_000002.10:g.215553513G>A | NCBI36 |
| NG_007074.1:g.162884C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272895.12:c.4679C>T MANE Select | ENSP00000272895.7:p.Ser1560Phe | |
| ENST00000272895.11:c.4679C>T | ENSP00000272895.7:p.Ser1560Phe | |
| ENST00000389661.4:c.3725C>T | ENSP00000374312.4:p.Ser1242Phe | |
| NM_015657.3:c.3725C>T | NP_056472.2:p.Ser1242Phe | |
| NM_173076.2:c.4679C>T | NP_775099.2:p.Ser1560Phe | |
| NR_103740.1:n.4979C>T | ||
| XM_011510951.1:c.4688C>T | XP_011509253.1:p.Ser1563Phe | |
| XM_011510952.1:c.4688C>T | XP_011509254.1:p.Ser1563Phe | |
| XM_011510951.2:c.4688C>T | XP_011509253.1:p.Ser1563Phe | |
| NM_173076.3:c.4679C>T MANE Select | NP_775099.2:p.Ser1560Phe | |
| NR_103740.2:n.5177C>T | ||
| NM_015657.4:c.3725C>T | NP_056472.2:p.Ser1242Phe |