Linked Data
gnomAD v4:
17-10404244-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.10404244A>T , CM000679.2:g.10404244A>T | GRCh38 |
| NC_000017.10:g.10307561A>T , CM000679.1:g.10307561A>T | GRCh37 |
| NC_000017.9:g.10248286A>T | NCBI36 |
| NG_013015.1:g.22707T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403437.2:c.2688+86T>A (MYH8) MANE Select | ENSP00000384330.2:n.2688+86T>A | |
| NM_002472.2:c.2688+86T>A (MYH8) | NP_002463.2:n.2688+86T>A | |
| NR_125367.1:n.77-1904A>T (MYHAS) | ||
| XM_011523873.1:c.2784+86T>A (MYH8) | XP_011522175.1:n.2784+86T>A | |
| XM_011523874.1:c.2784+86T>A (MYH8) | XP_011522176.1:n.2784+86T>A | |
| NM_002472.3:c.2688+86T>A (MYH8) MANE Select | NP_002463.2:n.2688+86T>A |