Linked Data
dbSNP Id:
rs772460139
ExAC:
16:4849786 G / C
gnomAD v2:
16-4849786-G-C
gnomAD v4:
16-4799785-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.4799785G>C , CM000678.2:g.4799785G>C | GRCh38 |
| NC_000016.9:g.4849786G>C , CM000678.1:g.4849786G>C | GRCh37 |
| NC_000016.8:g.4789787G>C | NCBI36 |
| NG_032174.1:g.8166C>G , LRG_455:g.8166C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322048.12:c.337-4C>G MANE Select | ENSP00000322832.6:n.337-4C>G | |
| ENST00000322048.11:c.337-4C>G | ENSP00000322832.5:n.337-4C>G | |
| ENST00000585653.1:n.469-4C>G | ||
| ENST00000586153.1:c.82-4C>G | ENSP00000464699.1:n.82-4C>G | |
| ENST00000586336.5:n.436-4C>G | ||
| ENST00000586504.5:c.117-4C>G | ||
| ENST00000587377.5:c.337-4C>G | ENSP00000468343.1:n.337-4C>G | |
| ENST00000587711.5:c.118-1118C>G | ENSP00000467459.1:n.118-1118C>G | |
| ENST00000587843.5:c.*75-4C>G | ENSP00000465970.1:n.*75-4C>G | |
| ENST00000588201.5:c.*194-4C>G | ENSP00000466529.1:n.*194-4C>G | |
| ENST00000589543.5:n.294-4C>G | ||
| ENST00000591292.5:n.1666-4C>G | ||
| ENST00000591392.5:c.265-4C>G | ENSP00000467509.1:n.265-4C>G | |
| ENST00000592019.1:c.56-4C>G | ||
| NM_024589.2:c.337-4C>G , LRG_455t1:c.337-4C>G | NP_078865.1:n.337-4C>G | |
| NR_046480.1:n.661-4C>G | ||
| XM_006720947.2:c.337-4C>G | XP_006721010.1:n.337-4C>G | |
| XM_006720948.2:c.67-4C>G | XP_006721011.1:n.67-4C>G | |
| XM_006720947.4:c.337-4C>G | XP_006721010.1:n.337-4C>G | |
| XM_006720948.4:c.67-4C>G | XP_006721011.1:n.67-4C>G | |
| NM_024589.3:c.337-4C>G MANE Select | NP_078865.1:n.337-4C>G | |
| NR_046480.2:n.344-4C>G |