Linked Data
gnomAD v4:
12-57764460-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764460T>C , CM000674.2:g.57764460T>C | GRCh38 |
| NC_000012.11:g.58158243T>C , CM000674.1:g.58158243T>C | GRCh37 |
| NC_000012.10:g.56444510T>C | NCBI36 |
| NG_007076.1:g.7734A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1135A>G | ENSP00000518840.1:p.Ser379Gly | |
| ENST00000713545.1:c.*59A>G | ENSP00000518841.1:n.*59A>G | |
| ENST00000228606.9:c.1054A>G MANE Select | ENSP00000228606.4:p.Ser352Gly | |
| ENST00000228606.8:c.1054A>G | ENSP00000228606.4:p.Ser352Gly | |
| ENST00000546567.5:c.349A>G | ENSP00000449472.1:p.Ser117Gly | |
| ENST00000547344.5:n.1193A>G | ||
| NM_000785.3:c.1054A>G | NP_000776.1:p.Ser352Gly | |
| NM_000785.4:c.1054A>G MANE Select | NP_000776.1:p.Ser352Gly |