Linked Data
dbSNP Id:
rs775049360
ExAC:
7:95818602 T / C
gnomAD v2:
7-95818602-T-C
gnomAD v3:
7-96189290-T-C
gnomAD v4:
7-96189290-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.96189290T>C , CM000669.2:g.96189290T>C | GRCh38 |
| NC_000007.13:g.95818602T>C , CM000669.1:g.95818602T>C | GRCh37 |
| NC_000007.12:g.95656538T>C | NCBI36 |
| NG_012247.1:g.137858A>G | |
| NG_012247.2:g.137858A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000265631.10:c.933+4A>G MANE Select | ENSP00000265631.6:n.933+4A>G | |
| ENST00000265631.9:c.933+4A>G | ENSP00000265631.5:n.933+4A>G | |
| ENST00000416240.6:c.933+4A>G | ENSP00000400101.2:n.933+4A>G | |
| ENST00000484495.5:n.86+4A>G | ||
| NM_001160210.1:c.933+4A>G | NP_001153682.1:n.933+4A>G | |
| NM_014251.2:c.933+4A>G | NP_055066.1:n.933+4A>G | |
| NR_027662.1:n.1008+4A>G | ||
| XM_006715831.2:c.966+4A>G | XP_006715894.1:n.966+4A>G | |
| XM_011515727.1:c.966+4A>G | XP_011514029.1:n.966+4A>G | |
| XM_011515728.1:c.81+4A>G | XP_011514030.1:n.81+4A>G | |
| XM_006715831.4:c.966+4A>G | XP_006715894.1:n.966+4A>G | |
| XM_011515727.3:c.966+4A>G | XP_011514029.1:n.966+4A>G | |
| XM_017011663.1:c.924+4A>G | XP_016867152.1:n.924+4A>G | |
| XM_017011664.2:c.81+4A>G | XP_016867153.1:n.81+4A>G | |
| XM_017011665.1:c.81+4A>G | XP_016867154.1:n.81+4A>G | |
| XR_001744525.2:n.1104+4A>G | ||
| XR_002956405.1:n.1246+4A>G | ||
| NM_014251.3:c.933+4A>G MANE Select | NP_055066.1:n.933+4A>G | |
| NR_027662.2:n.959+4A>G | ||
| NM_001160210.2:c.933+4A>G | NP_001153682.1:n.933+4A>G |