Linked Data
gnomAD v4:
4-4860353-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.4860353T>C , CM000666.2:g.4860353T>C | GRCh38 |
| NC_000004.11:g.4862080T>C , CM000666.1:g.4862080T>C | GRCh37 |
| NC_000004.10:g.4912981T>C | NCBI36 |
| NG_008121.1:g.5689T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382723.5:c.454T>C MANE Select | ENSP00000372170.4:p.Ser152Pro | |
| ENST00000382723.4:c.454T>C | ENSP00000372170.4:p.Ser152Pro | |
| NM_002448.3:c.454T>C MANE Select | NP_002439.2:p.Ser152Pro |