Linked Data
MyVariant Identifiers:
chr15:g.41223903G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40931705G>C , CM000677.2:g.40931705G>C | GRCh38 |
| NC_000015.9:g.41223903G>C , CM000677.1:g.41223903G>C | GRCh37 |
| NC_000015.8:g.39011195G>C | NCBI36 |
| NG_046974.1:g.7373G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000249749.7:c.597G>C MANE Select | ENSP00000249749.5:p.Val199= | |
| ENST00000249749.6:c.597G>C | ENSP00000249749.5:p.Val199= | |
| ENST00000559440.1:n.826G>C | ||
| NM_019074.3:c.597G>C | NP_061947.1:p.Val199= | |
| NM_019074.4:c.597G>C MANE Select | NP_061947.1:p.Val199= |