Linked Data
dbSNP Id:
rs1271561718
gnomAD v2:
3-48607663-G-A
gnomAD v3:
3-48570230-G-A
gnomAD v4:
3-48570230-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.48570230G>A , CM000665.2:g.48570230G>A | GRCh38 |
| NC_000003.11:g.48607663G>A , CM000665.1:g.48607663G>A | GRCh37 |
| NC_000003.10:g.48582667G>A | NCBI36 |
| NG_007065.1:g.30023C>T , LRG_286:g.30023C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000681320.1:c.7440+45C>T MANE Select | ENSP00000506558.1:n.7440+45C>T | |
| ENST00000328333.12:c.7440+45C>T | ENSP00000332371.8:n.7440+45C>T | |
| ENST00000422991.1:c.435+45C>T | ENSP00000391608.1:n.435+45C>T | |
| ENST00000459756.5:n.212C>T | ||
| ENST00000467985.1:n.235C>T | ||
| ENST00000487017.5:n.4079+45C>T | ||
| NM_000094.3:c.7440+45C>T , LRG_286t1:c.7440+45C>T | NP_000085.1:n.7440+45C>T | |
| XM_011533336.1:c.7467+45C>T | XP_011531638.1:n.7467+45C>T | |
| XM_011533337.1:c.7440+45C>T | XP_011531639.1:n.7440+45C>T | |
| XM_011533338.1:c.7408-52C>T | XP_011531640.1:n.7408-52C>T | |
| XM_011533339.1:c.7467+45C>T | XP_011531641.1:n.7467+45C>T | |
| XM_011533340.1:c.7430C>T | XP_011531642.1:p.Ser2477Phe | |
| XM_011533341.1:c.7404C>T | XP_011531643.1:p.Leu2468= | |
| XM_011533342.1:c.7382-52C>T | XP_011531644.1:n.7382-52C>T | |
| XR_940369.1:n.7503+45C>T | ||
| XR_940370.1:n.7503+45C>T | ||
| XR_940371.1:n.7503+45C>T | ||
| XR_940372.1:n.7477+45C>T | ||
| XM_017005688.1:c.7381-52C>T | XP_016861177.1:n.7381-52C>T | |
| XM_017005689.1:c.7440+45C>T | XP_016861178.1:n.7440+45C>T | |
| XM_017005690.1:c.7403C>T | XP_016861179.1:p.Ser2468Phe | |
| XM_017005691.1:c.7377C>T | XP_016861180.1:p.Leu2459= | |
| XM_017005692.1:c.7355-52C>T | XP_016861181.1:n.7355-52C>T | |
| XR_001740003.1:n.7476+45C>T | ||
| XR_001740004.1:n.7476+45C>T | ||
| XR_001740005.1:n.7476+45C>T | ||
| XR_001740006.1:n.7450+45C>T | ||
| NM_000094.4:c.7440+45C>T MANE Select | NP_000085.1:n.7440+45C>T |