Linked Data
dbSNP Id:
rs1381818875
gnomAD v2:
17-38028713-C-T
gnomAD v3:
17-39872460-C-T
gnomAD v4:
17-39872460-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.39872460C>T , CM000679.2:g.39872460C>T | GRCh38 |
| NC_000017.10:g.38028713C>T , CM000679.1:g.38028713C>T | GRCh37 |
| NC_000017.9:g.35282239C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000348931.9:c.597C>T MANE Select | ENSP00000335384.5:p.Leu199= | |
| ENST00000348931.8:c.597C>T | ENSP00000335384.5:p.Leu199= | |
| ENST00000377940.3:c.531C>T | ENSP00000367174.3:p.Leu177= | |
| ENST00000583811.5:c.243C>T | ENSP00000462463.1:p.Leu81= | |
| ENST00000584588.5:c.407-584C>T | ENSP00000462067.1:n.407-584C>T | |
| NM_198844.2:c.531C>T | NP_942141.2:p.Leu177= | |
| NM_199321.2:c.597C>T | NP_955353.1:p.Leu199= | |
| XM_011524298.1:c.597C>T | XP_011522600.1:p.Leu199= | |
| XR_002957959.1:n.788C>T | ||
| NM_198844.3:c.531C>T | NP_942141.2:p.Leu177= | |
| NM_199321.3:c.597C>T MANE Select | NP_955353.1:p.Leu199= |