Linked Data
dbSNP Id:
rs116840758
gnomAD v2:
7-42007193-C-T
gnomAD v4:
7-41967595-C-T
PubMed:
PMID:20301638
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41967595C>T , CM000669.2:g.41967595C>T | GRCh38 |
| NC_000007.13:g.42007193C>T , CM000669.1:g.42007193C>T | GRCh37 |
| NC_000007.12:g.41973718C>T | NCBI36 |
| NG_008434.1:g.274426G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000395925.8:c.2431+1G>A MANE Select | ENSP00000379258.3:n.2431+1G>A | |
| ENST00000677288.1:c.2257+1G>A | ENSP00000503986.1:n.2257+1G>A | |
| ENST00000677605.1:c.2431+1G>A | ENSP00000503743.1:n.2431+1G>A | |
| ENST00000678429.1:c.2431+1G>A | ENSP00000502957.1:n.2431+1G>A | |
| ENST00000395925.7:c.2431+1G>A | ENSP00000379258.3:n.2431+1G>A | |
| ENST00000479210.1:n.2408+1G>A | ||
| NM_000168.5:c.2431+1G>A | NP_000159.3:n.2431+1G>A | |
| XM_005249703.1:c.2431+1G>A | XP_005249760.1:n.2431+1G>A | |
| XM_005249704.2:c.2431+1G>A | XP_005249761.1:n.2431+1G>A | |
| XM_011515272.1:c.2431+1G>A | XP_011513574.1:n.2431+1G>A | |
| XM_011515273.1:c.2431+1G>A | XP_011513575.1:n.2431+1G>A | |
| XM_011515274.1:c.2254+1G>A | XP_011513576.1:n.2254+1G>A | |
| XM_011515274.2:c.2254+1G>A | XP_011513576.1:n.2254+1G>A | |
| XM_017011997.1:c.2428+1G>A | XP_016867486.1:n.2428+1G>A | |
| NM_000168.6:c.2431+1G>A MANE Select | NP_000159.3:n.2431+1G>A |