Linked Data
gnomAD v4:
9-137199478-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137199478T>C , CM000671.2:g.137199478T>C | GRCh38 |
| NC_000009.11:g.140093930T>C , CM000671.1:g.140093930T>C | GRCh37 |
| NC_000009.10:g.139213751T>C | NCBI36 |
| NG_027801.1:g.6234A>G | |
| NG_027801.2:g.9716A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409012.6:c.1234A>G MANE Select | ENSP00000387100.4:p.Arg412Gly | |
| ENST00000333046.8:c.628A>G | ENSP00000327617.4:p.Arg210Gly | |
| ENST00000409012.4:c.1234A>G | ENSP00000387100.4:p.Arg412Gly | |
| ENST00000541945.1:n.90+4626A>G | ||
| NM_001128228.2:c.1234A>G | NP_001121700.2:p.Arg412Gly | |
| NM_001128228.3:c.1234A>G MANE Select | NP_001121700.2:p.Arg412Gly |