Linked Data
gnomAD v4:
19-48703620-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48703620T>A , CM000681.2:g.48703620T>A | GRCh38 |
| NC_000019.9:g.49206877T>A , CM000681.1:g.49206877T>A | GRCh37 |
| NC_000019.8:g.53898689T>A | NCBI36 |
| NG_007511.1:g.12650T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000425340.3:c.664T>A MANE Select | ENSP00000387498.2:p.Tyr222Asn | |
| ENST00000522966.2:c.664T>A | ENSP00000430227.2:p.Tyr222Asn | |
| ENST00000391876.5:c.664T>A | ENSP00000375748.4:p.Tyr222Asn | |
| ENST00000425340.2:c.664T>A | ENSP00000387498.2:p.Tyr222Asn | |
| NM_000511.5:c.664T>A | NP_000502.4:p.Tyr222Asn | |
| NM_001097638.2:c.664T>A | NP_001091107.1:p.Tyr222Asn | |
| NR_131188.1:n.229A>T | ||
| NM_000511.6:c.664T>A MANE Select | NP_000502.4:p.Tyr222Asn | |
| NM_001097638.3:c.664T>A | NP_001091107.1:p.Tyr222Asn |