Linked Data
gnomAD v4:
19-4816766-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.4816766C>A , CM000681.2:g.4816766C>A | GRCh38 |
| NC_000019.9:g.4816778C>A , CM000681.1:g.4816778C>A | GRCh37 |
| NC_000019.8:g.4767778C>A | NCBI36 |
| NG_031998.1:g.19977G>T , LRG_358:g.19977G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248244.6:c.1612G>T MANE Select | ENSP00000248244.4:p.Ala538Ser | |
| ENST00000248244.5:c.1612G>T | ENSP00000248244.4:p.Ala538Ser | |
| ENST00000621756.1:c.1195G>T | ENSP00000479467.1:p.Ala399Ser | |
| NM_182919.3:c.1612G>T , LRG_358t1:c.1612G>T | NP_891549.1:p.Ala538Ser | |
| NM_001385678.1:c.1570G>T | NP_001372607.1:p.Ala524Ser | |
| NM_001385679.1:c.1477G>T | NP_001372608.1:p.Ala493Ser | |
| NM_001385680.1:c.970G>T | NP_001372609.1:p.Ala324Ser | |
| NM_182919.4:c.1612G>T MANE Select | NP_891549.1:p.Ala538Ser |