Linked Data
gnomAD v3:
16-1790777-C-G
gnomAD v4:
16-1790777-C-G
MyVariant Identifiers:
chr16:g.1840778C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1790777C>G , CM000678.2:g.1790777C>G | GRCh38 |
| NC_000016.9:g.1840778C>G , CM000678.1:g.1840778C>G | GRCh37 |
| NC_000016.8:g.1780779C>G | NCBI36 |
| NG_011778.1:g.7957G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215539.4:c.1641G>C (IGFALS) MANE Select | ENSP00000215539.3:p.Leu547= | |
| ENST00000215539.3:c.1641G>C (IGFALS) | ENSP00000215539.3:p.Leu547= | |
| ENST00000415638.3:c.1755G>C (IGFALS) | ENSP00000416683.3:p.Leu585= | |
| ENST00000569769.1:c.-13+2860G>C (SPSB3) | ENSP00000455098.1:n.-13+2860G>C | |
| NM_001146006.1:c.1755G>C (IGFALS) | NP_001139478.1:p.Leu585= | |
| NM_004970.2:c.1641G>C (IGFALS) | NP_004961.1:p.Leu547= | |
| NR_027389.1:n.1695G>C (IGFALS) | ||
| XM_011522476.1:c.1722G>C (IGFALS) | XP_011520778.1:p.Leu574= | |
| NM_001146006.2:c.1755G>C (IGFALS) | NP_001139478.1:p.Leu585= | |
| NM_004970.3:c.1641G>C (IGFALS) MANE Select | NP_004961.1:p.Leu547= |