Linked Data
dbSNP Id:
rs1415148
gnomAD v2:
1-150705755-G-A
gnomAD v3:
1-150733279-G-A
gnomAD v4:
1-150733279-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.150733279G>A , CM000663.2:g.150733279G>A | GRCh38 |
| NC_000001.10:g.150705755G>A , CM000663.1:g.150705755G>A | GRCh37 |
| NC_000001.9:g.148972379G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368985.8:c.897-134C>T MANE Select | ENSP00000357981.3:n.897-134C>T | |
| ENST00000448301.7:c.669-134C>T | ENSP00000408414.2:n.669-134C>T | |
| ENST00000472977.7:c.897-134C>T | ENSP00000475176.2:n.897-134C>T | |
| ENST00000483930.2:c.*91-134C>T | ENSP00000475812.2:n.*91-134C>T | |
| ENST00000607427.2:c.897-134C>T | ENSP00000475557.2:n.897-134C>T | |
| ENST00000679512.1:c.794-134C>T | ENSP00000505113.1:n.794-134C>T | |
| ENST00000679898.1:c.624-134C>T | ENSP00000505326.1:n.624-134C>T | |
| ENST00000680288.1:c.747-134C>T | ENSP00000506001.1:n.747-134C>T | |
| ENST00000680311.1:c.628-134C>T | ENSP00000505020.1:n.628-134C>T | |
| ENST00000680471.1:c.*68-134C>T | ENSP00000506603.1:n.*68-134C>T | |
| ENST00000680664.1:c.720-134C>T | ENSP00000506248.1:n.720-134C>T | |
| ENST00000680931.1:c.*247-134C>T | ENSP00000504934.1:n.*247-134C>T | |
| ENST00000681357.1:n.287-134C>T | ||
| ENST00000681444.1:c.897-134C>T | ENSP00000505359.1:n.897-134C>T | |
| ENST00000368985.7:c.897-134C>T | ENSP00000357981.3:n.897-134C>T | |
| ENST00000448301.6:c.747-134C>T | ENSP00000408414.1:n.747-134C>T | |
| ENST00000472977.6:c.190-134C>T | ||
| ENST00000483930.1:c.445-134C>T | ENSP00000475812.1:n.445-134C>T | |
| NM_001199739.1:c.747-134C>T | NP_001186668.1:n.747-134C>T | |
| NM_004079.4:c.897-134C>T | NP_004070.3:n.897-134C>T | |
| NM_004079.5:c.897-134C>T MANE Select | NP_004070.3:n.897-134C>T | |
| NM_001199739.2:c.747-134C>T | NP_001186668.1:n.747-134C>T |