Linked Data
dbSNP Id:
rs371047361
ExAC:
17:42449798 G / T
gnomAD v2:
17-42449798-G-T
gnomAD v3:
17-44372430-G-T
gnomAD v4:
17-44372430-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44372430G>T , CM000679.2:g.44372430G>T | GRCh38 |
| NC_000017.10:g.42449798G>T , CM000679.1:g.42449798G>T | GRCh37 |
| NC_000017.9:g.39805324G>T | NCBI36 |
| NG_008331.1:g.22076C>A , LRG_479:g.22076C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.3061-7C>A MANE Select | ENSP00000262407.5:n.3061-7C>A | |
| ENST00000648408.1:c.2375-7C>A | ||
| ENST00000262407.5:c.3061-7C>A | ENSP00000262407.5:n.3061-7C>A | |
| ENST00000587295.5:c.254-7C>A | ||
| ENST00000588098.1:c.38-7C>A | ||
| NM_000419.3:c.3061-7C>A , LRG_479t1:c.3061-7C>A | NP_000410.2:n.3061-7C>A | |
| XM_011524749.1:c.2959-7C>A | XP_011523051.1:n.2959-7C>A | |
| XM_011524750.1:c.2944-7C>A | XP_011523052.1:n.2944-7C>A | |
| NM_000419.4:c.3061-7C>A | NP_000410.2:n.3061-7C>A | |
| NM_000419.5:c.3061-7C>A MANE Select | NP_000410.2:n.3061-7C>A |