Linked Data
dbSNP Id:
rs371195304
ExAC:
16:1411959 G / C
gnomAD v2:
16-1411959-G-C
gnomAD v4:
16-1361958-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1361958G>C , CM000678.2:g.1361958G>C | GRCh38 |
| NC_000016.9:g.1411959G>C , CM000678.1:g.1411959G>C | GRCh37 |
| NC_000016.8:g.1351960G>C | NCBI36 |
| NG_016985.1:g.15060G>C | |
| NG_033129.1:g.57747C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000527168.6:n.416+3G>C | ||
| ENST00000529110.2:c.401+3G>C | ENSP00000435349.2:n.401+3G>C | |
| ENST00000529957.6:n.375+3G>C | ||
| ENST00000683366.1:c.*49+3G>C | ENSP00000507283.1:n.*49+3G>C | |
| ENST00000683887.1:c.365+3G>C | ENSP00000506886.1:n.365+3G>C | |
| ENST00000684100.1:n.311+3G>C | ||
| ENST00000684126.1:n.375+3G>C | ||
| ENST00000684688.1:n.942+3G>C | ||
| ENST00000204679.9:c.317+3G>C MANE Select | ENSP00000204679.4:n.317+3G>C | |
| ENST00000204679.8:c.317+3G>C | ENSP00000204679.4:n.317+3G>C | |
| ENST00000526820.5:c.*219+3G>C | ENSP00000434413.1:n.*219+3G>C | |
| ENST00000527076.1:n.1333+3G>C | ||
| ENST00000527168.5:n.353+3G>C | ||
| ENST00000529110.1:c.384+3G>C | ||
| ENST00000529957.5:n.416+3G>C | ||
| NM_032520.4:c.317+3G>C | NP_115909.1:n.317+3G>C | |
| XM_017023782.1:c.365+3G>C | XP_016879271.1:n.365+3G>C | |
| XM_017023783.1:c.-44+3G>C | XP_016879272.1:n.-44+3G>C | |
| NM_032520.5:c.317+3G>C MANE Select | NP_115909.1:n.317+3G>C |