Linked Data
gnomAD v4:
6-32443837-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32443837T>C , CM000668.2:g.32443837T>C | GRCh38 |
| NC_000006.11:g.32411614T>C , CM000668.1:g.32411614T>C | GRCh37 |
| NC_000006.10:g.32519592T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395388.7:c.692T>C MANE Select | ENSP00000378786.2:p.Ile231Thr | |
| ENST00000374982.5:c.617T>C | ENSP00000364121.5:p.Ile206Thr | |
| ENST00000395388.6:c.692T>C | ENSP00000378786.2:p.Ile231Thr | |
| NM_019111.4:c.692T>C | NP_061984.2:p.Ile231Thr | |
| NM_019111.5:c.692T>C MANE Select | NP_061984.2:p.Ile231Thr |