Linked Data
gnomAD v4:
9-133644273-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133644273G>C , CM000671.2:g.133644273G>C | GRCh38 |
| NC_000009.11:g.136509395G>C , CM000671.1:g.136509395G>C | GRCh37 |
| NC_000009.10:g.135499216G>C | NCBI36 |
| NG_008645.1:g.12911G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393056.8:c.977G>C MANE Select | ENSP00000376776.2:p.Arg326Thr | |
| ENST00000393056.6:c.977G>C | ENSP00000376776.2:p.Arg326Thr | |
| NM_000787.3:c.977G>C | NP_000778.3:p.Arg326Thr | |
| NM_000787.4:c.977G>C MANE Select | NP_000778.3:p.Arg326Thr |