Linked Data
gnomAD v4:
8-19956042-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19956042G>C , CM000670.2:g.19956042G>C | GRCh38 |
| NC_000008.10:g.19813553G>C , CM000670.1:g.19813553G>C | GRCh37 |
| NC_000008.9:g.19857833G>C | NCBI36 |
| NG_008855.1:g.21972G>C | |
| NG_008855.2:g.59326G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.977G>C MANE Select | ENSP00000497642.1:p.Ser326Thr | |
| ENST00000650478.1:c.38G>C | ENSP00000497560.1:p.Ser13Thr | |
| ENST00000311322.8:c.977G>C | ENSP00000309757.6:p.Ser326Thr | |
| NM_000237.2:c.977G>C | NP_000228.1:p.Ser326Thr | |
| NM_000237.3:c.977G>C MANE Select | NP_000228.1:p.Ser326Thr |