Linked Data
dbSNP Id:
rs891935536
gnomAD v2:
6-24205170-A-C
gnomAD v3:
6-24204942-A-C
gnomAD v4:
6-24204942-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.24204942A>C , CM000668.2:g.24204942A>C | GRCh38 |
| NC_000006.11:g.24205170A>C , CM000668.1:g.24205170A>C | GRCh37 |
| NC_000006.10:g.24313149A>C | NCBI36 |
| NG_012829.1:g.158111T>G | |
| NG_012829.2:g.183351T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378454.8:c.1023+60T>G MANE Select | ENSP00000367715.3:n.1023+60T>G | |
| ENST00000378450.6:c.282+60T>G | ENSP00000367711.3:n.282+60T>G | |
| ENST00000378454.7:c.1023+60T>G | ENSP00000367715.3:n.1023+60T>G | |
| NM_001195610.1:c.1023+60T>G | NP_001182539.1:n.1023+60T>G | |
| NM_016356.4:c.1023+60T>G | NP_057440.2:n.1023+60T>G | |
| NM_016356.5:c.1023+60T>G MANE Select | NP_057440.2:n.1023+60T>G | |
| NM_001195610.2:c.1023+60T>G | NP_001182539.1:n.1023+60T>G |