Linked Data
gnomAD v4:
19-18787647-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.18787647T>C , CM000681.2:g.18787647T>C | GRCh38 |
| NC_000019.9:g.18898456T>C , CM000681.1:g.18898456T>C | GRCh37 |
| NC_000019.8:g.18759456T>C | NCBI36 |
| NG_007070.1:g.8659A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000222271.7:c.979A>G MANE Select | ENSP00000222271.2:p.Asn327Asp | |
| ENST00000222271.6:c.979A>G | ENSP00000222271.2:p.Asn327Asp | |
| ENST00000425807.1:c.820A>G | ENSP00000403792.1:p.Asn274Asp | |
| ENST00000542601.6:c.880A>G | ENSP00000439156.2:p.Asn294Asp | |
| NM_000095.2:c.979A>G | NP_000086.2:p.Asn327Asp | |
| NM_000095.3:c.979A>G MANE Select | NP_000086.2:p.Asn327Asp |