Linked Data
gnomAD v4:
19-7527576-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7527576A>C , CM000681.2:g.7527576A>C | GRCh38 |
| NC_000019.9:g.7592462A>C , CM000681.1:g.7592462A>C | GRCh37 |
| NC_000019.8:g.7498462A>C | NCBI36 |
| NG_015806.1:g.9967A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.628A>C MANE Select | ENSP00000264079.5:p.Thr210Pro | |
| ENST00000264079.10:c.628A>C | ENSP00000264079.5:p.Thr210Pro | |
| ENST00000394321.9:n.708A>C | ||
| ENST00000598406.1:n.449A>C | ||
| ENST00000601003.1:c.572-288A>C | ENSP00000469074.1:n.572-288A>C | |
| NM_020533.2:c.628A>C | NP_065394.1:p.Thr210Pro | |
| NM_020533.3:c.628A>C MANE Select | NP_065394.1:p.Thr210Pro |