Linked Data
dbSNP Id:
rs2055278840
gnomAD v4:
16-56884155-C-G
MyVariant Identifiers:
chr16:g.56918067C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56884155C>G , CM000678.2:g.56884155C>G | GRCh38 |
| NC_000016.9:g.56918067C>G , CM000678.1:g.56918067C>G | GRCh37 |
| NC_000016.8:g.55475568C>G | NCBI36 |
| NG_009386.1:g.23949C>G | |
| NG_009386.2:g.23949C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000563236.6:c.1776C>G MANE Select | ENSP00000456149.2:p.Ala592= | |
| ENST00000262502.5:c.1773C>G | ENSP00000262502.5:p.Ala591= | |
| ENST00000438926.6:c.1776C>G | ENSP00000402152.2:p.Ala592= | |
| ENST00000563236.5:c.1776C>G | ENSP00000456149.1:p.Ala592= | |
| ENST00000566786.5:c.1773C>G | ENSP00000457552.1:p.Ala591= | |
| NM_000339.2:c.1776C>G | NP_000330.2:p.Ala592= | |
| NM_001126107.1:c.1773C>G | NP_001119579.1:p.Ala591= | |
| NM_001126108.1:c.1776C>G | NP_001119580.1:p.Ala592= | |
| XM_005256119.1:c.1773C>G | XP_005256176.1:p.Ala591= | |
| XM_005256119.2:c.1773C>G | XP_005256176.1:p.Ala591= | |
| NM_000339.3:c.1776C>G | NP_000330.3:p.Ala592= | |
| NM_001126107.2:c.1773C>G | NP_001119579.2:p.Ala591= | |
| NM_001126108.2:c.1776C>G MANE Select | NP_001119580.2:p.Ala592= |