Linked Data
dbSNP Id:
rs1266123570
gnomAD v2:
16-3777960-G-A
gnomAD v4:
16-3727959-G-A
COSMIC:
COSM231338
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3727959G>A , CM000678.2:g.3727959G>A | GRCh38 |
| NC_000016.9:g.3777960G>A , CM000678.1:g.3777960G>A | GRCh37 |
| NC_000016.8:g.3717961G>A | NCBI36 |
| NG_009873.1:g.157162C>T | |
| NG_009873.2:g.157755C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262367.10:c.7088C>T MANE Select | ENSP00000262367.5:p.Pro2363Leu | |
| ENST00000262367.9:c.7088C>T | ENSP00000262367.5:p.Pro2363Leu | |
| ENST00000382070.7:c.6974C>T | ENSP00000371502.3:p.Pro2325Leu | |
| NM_001079846.1:c.6974C>T | NP_001073315.1:p.Pro2325Leu | |
| NM_004380.2:c.7088C>T | NP_004371.2:p.Pro2363Leu | |
| XM_005255124.3:c.7043C>T | XP_005255181.1:p.Pro2348Leu | |
| XM_005255125.3:c.6671C>T | XP_005255182.1:p.Pro2224Leu | |
| XM_006720848.2:c.6827C>T | XP_006720911.1:p.Pro2276Leu | |
| XM_011522380.1:c.7034C>T | XP_011520682.1:p.Pro2345Leu | |
| XM_011522381.1:c.6335C>T | XP_011520683.1:p.Pro2112Leu | |
| XM_005255124.4:c.7043C>T | XP_005255181.1:p.Pro2348Leu | |
| XM_005255125.4:c.6671C>T | XP_005255182.1:p.Pro2224Leu | |
| XM_006720848.3:c.6827C>T | XP_006720911.1:p.Pro2276Leu | |
| XM_011522381.2:c.6335C>T | XP_011520683.1:p.Pro2112Leu | |
| XM_017022944.1:c.7082C>T | XP_016878433.1:p.Pro2361Leu | |
| NM_004380.3:c.7088C>T MANE Select | NP_004371.2:p.Pro2363Leu |