Linked Data
dbSNP Id:
rs545736655
gnomAD v2:
5-131720879-C-T
gnomAD v3:
5-132385187-C-T
gnomAD v4:
5-132385187-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132385187C>T , CM000667.2:g.132385187C>T | GRCh38 |
| NC_000005.9:g.131720879C>T , CM000667.1:g.131720879C>T | GRCh37 |
| NC_000005.8:g.131748778C>T | NCBI36 |
| NG_008982.1:g.20479C>T | |
| NG_008982.2:g.20484C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000415928.6:c.665+873C>T | ENSP00000388838.2:n.665+873C>T | |
| ENST00000435065.7:c.725-141C>T | ENSP00000402760.2:n.725-141C>T | |
| ENST00000448810.6:c.653-141C>T | ENSP00000401860.2:n.653-141C>T | |
| ENST00000686757.1:c.672-141C>T | ENSP00000510721.1:n.672-141C>T | |
| ENST00000687740.1:n.1672C>T | ||
| ENST00000688151.1:n.1845-141C>T | ||
| ENST00000689271.1:c.671+867C>T | ENSP00000510797.1:n.671+867C>T | |
| ENST00000690900.1:c.672-189C>T | ENSP00000510703.1:n.672-189C>T | |
| ENST00000692212.1:n.338C>T | ||
| ENST00000692355.1:c.204+886C>T | ||
| ENST00000692413.1:c.672-141C>T | ENSP00000509374.1:n.672-141C>T | |
| ENST00000692825.1:c.721-141C>T | ENSP00000509447.1:n.721-141C>T | |
| ENST00000693308.1:c.666-141C>T | ENSP00000509770.1:n.666-141C>T | |
| ENST00000693763.1:n.1672C>T | ||
| ENST00000245407.8:c.653-141C>T MANE Select | ENSP00000245407.3:n.653-141C>T | |
| ENST00000245407.7:c.653-141C>T | ENSP00000245407.3:n.653-141C>T | |
| ENST00000415928.5:c.422-141C>T | ENSP00000388838.1:n.422-141C>T | |
| ENST00000435065.6:c.725-141C>T | ENSP00000402760.2:n.725-141C>T | |
| ENST00000437841.6:c.394-141C>T | ENSP00000400553.1:n.394-141C>T | |
| ENST00000461013.5:n.8075-141C>T | ||
| NM_001308122.1:c.725-141C>T | NP_001295051.1:n.725-141C>T | |
| NM_003060.3:c.653-141C>T | NP_003051.1:n.653-141C>T | |
| XM_011543590.1:c.35-141C>T | XP_011541892.1:n.35-141C>T | |
| XR_427718.1:n.1013-141C>T | ||
| XR_948290.1:n.994-141C>T | ||
| XR_948291.1:n.1007-141C>T | ||
| XM_011543590.2:c.35-141C>T | XP_011541892.1:n.35-141C>T | |
| XM_017009778.2:c.125-141C>T | XP_016865267.1:n.125-141C>T | |
| XR_001742215.1:n.994-141C>T | ||
| XR_001742216.1:n.1013-141C>T | ||
| XR_427718.2:n.1013-141C>T | ||
| XR_948290.2:n.994-141C>T | ||
| XR_948291.2:n.1007-141C>T | ||
| NM_003060.4:c.653-141C>T MANE Select | NP_003051.1:n.653-141C>T | |
| NM_001308122.2:c.725-141C>T | NP_001295051.1:n.725-141C>T |