Linked Data
gnomAD v4:
19-694905-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.694905C>T , CM000681.2:g.694905C>T | GRCh38 |
| NC_000019.9:g.694905C>T , CM000681.1:g.694905C>T | GRCh37 |
| NC_000019.8:g.645905C>T | NCBI36 |
| NG_051189.1:g.5627G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000329267.9:c.142G>A MANE Select | ENSP00000327386.6:p.Ala48Thr | |
| ENST00000329267.8:c.142G>A | ENSP00000327386.6:p.Ala48Thr | |
| ENST00000613411.4:c.145G>A | ENSP00000482358.1:p.Ala49Thr | |
| NM_001308209.1:c.142G>A | NP_001295138.1:p.Ala48Thr | |
| NM_214710.3:c.145G>A | NP_999875.1:p.Ala49Thr | |
| NM_214710.4:c.145G>A | NP_999875.1:p.Ala49Thr | |
| NM_001308209.2:c.142G>A MANE Select | NP_001295138.2:p.Ala48Thr | |
| NM_214710.5:c.145G>A | NP_999875.2:p.Ala49Thr |