Linked Data
dbSNP Id:
rs546363204
gnomAD v2:
9-101142785-C-T
gnomAD v3:
9-98380503-C-T
gnomAD v4:
9-98380503-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98380503C>T , CM000671.2:g.98380503C>T | GRCh38 |
| NC_000009.11:g.101142785C>T , CM000671.1:g.101142785C>T | GRCh37 |
| NC_000009.10:g.100182606C>T | NCBI36 |
| NG_016426.1:g.333695G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000259455.4:c.1662+5137G>A MANE Select | ENSP00000259455.2:n.1662+5137G>A | |
| ENST00000637410.1:n.1440+5137G>A | ||
| ENST00000259455.3:c.1662+5137G>A | ENSP00000259455.2:n.1662+5137G>A | |
| ENST00000634314.1:n.167+5137G>A | ||
| NM_005458.7:c.1662+5137G>A | NP_005449.5:n.1662+5137G>A | |
| XM_005252316.3:c.888+5137G>A | XP_005252373.1:n.888+5137G>A | |
| XM_005252316.5:c.888+5137G>A | XP_005252373.1:n.888+5137G>A | |
| XM_017015331.2:c.1368+5137G>A | XP_016870820.1:n.1368+5137G>A | |
| XM_017015332.2:c.888+5137G>A | XP_016870821.1:n.888+5137G>A | |
| NM_005458.8:c.1662+5137G>A MANE Select | NP_005449.5:n.1662+5137G>A |