Linked Data
dbSNP Id:
rs1972182229
gnomAD v3:
19-29702880-C-T
gnomAD v4:
19-29702880-C-T
MyVariant Identifiers:
chr19:g.30193787C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.29702880C>T , CM000681.2:g.29702880C>T | GRCh38 |
| NC_000019.9:g.30193787C>T , CM000681.1:g.30193787C>T | GRCh37 |
| NC_000019.8:g.34885627C>T | NCBI36 |
| NG_031970.1:g.17910G>A | |
| NG_031970.2:g.17910G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000614091.5:c.258G>A | ENSP00000482097.2:p.Gln86= | |
| ENST00000623113.3:c.258G>A | ENSP00000485413.2:p.Gln86= | |
| ENST00000323670.14:c.258G>A MANE Select | ENSP00000313332.9:p.Gln86= | |
| ENST00000323670.13:c.258G>A | ENSP00000313332.8:p.Gln86= | |
| ENST00000342680.5:c.*172G>A | ENSP00000345497.5:n.*172G>A | |
| ENST00000392275.1:n.649G>A | ||
| ENST00000392276.1:c.66G>A | ENSP00000376102.1:p.Gln22= | |
| ENST00000392278.2:c.291G>A | ENSP00000376103.2:p.Gln97= | |
| ENST00000591243.1:c.258G>A | ENSP00000467516.1:p.Gln86= | |
| ENST00000592153.5:c.258G>A | ENSP00000467117.1:p.Gln86= | |
| ENST00000614091.4:c.258G>A | ENSP00000482097.1:p.Gln86= | |
| ENST00000623113.1:c.66G>A | ENSP00000485413.1:p.Gln22= | |
| NM_001031726.3:c.291G>A | NP_001026896.2:p.Gln97= | |
| NM_001256046.1:c.258G>A | NP_001242975.1:p.Gln86= | |
| NM_001256047.1:c.258G>A | NP_001242976.1:p.Gln86= | |
| NM_001282929.1:c.66G>A | NP_001269858.1:p.Gln22= | |
| NM_001282930.1:c.66G>A | NP_001269859.1:p.Gln22= | |
| NM_001282931.1:c.66G>A | NP_001269860.1:p.Gln22= | |
| NM_031448.4:c.258G>A | NP_113636.2:p.Gln86= | |
| XM_024451734.1:c.420G>A | XP_024307502.1:p.Gln140= | |
| XM_024451735.1:c.258G>A | XP_024307503.1:p.Gln86= | |
| XM_024451736.1:c.258G>A | XP_024307504.1:p.Gln86= | |
| XM_024451737.1:c.258G>A | XP_024307505.1:p.Gln86= | |
| XM_024451738.1:c.258G>A | XP_024307506.1:p.Gln86= | |
| NM_001256046.2:c.258G>A | NP_001242975.1:p.Gln86= | |
| NM_001282930.2:c.66G>A | NP_001269859.1:p.Gln22= | |
| NM_001282931.2:c.66G>A | NP_001269860.1:p.Gln22= | |
| NM_031448.6:c.258G>A MANE Select | NP_113636.2:p.Gln86= | |
| NM_001031726.4:c.258G>A | NP_001026896.3:p.Gln86= | |
| NM_001256046.3:c.258G>A | NP_001242975.1:p.Gln86= | |
| NM_001256047.2:c.258G>A | NP_001242976.1:p.Gln86= | |
| NM_001282930.3:c.66G>A | NP_001269859.1:p.Gln22= | |
| NM_001282931.3:c.66G>A | NP_001269860.1:p.Gln22= |