Linked Data
MyVariant Identifiers:
chr17:g.40696202G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42544184G>C , CM000679.2:g.42544184G>C | GRCh38 |
| NC_000017.10:g.40696202G>C , CM000679.1:g.40696202G>C | GRCh37 |
| NC_000017.9:g.37949728G>C | NCBI36 |
| NG_011552.1:g.13252G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.2178G>C MANE Select | ENSP00000225927.1:p.Leu726= | |
| ENST00000225927.6:c.2178G>C | ENSP00000225927.1:p.Leu726= | |
| NM_000263.3:c.2178G>C | NP_000254.2:p.Leu726= | |
| XM_006721920.2:c.1347G>C | XP_006721983.1:p.Leu449= | |
| XM_011524840.1:c.1179G>C | XP_011523142.1:p.Leu393= | |
| XM_017024687.1:c.1347G>C | XP_016880176.1:p.Leu449= | |
| XM_024450771.1:c.2235G>C | XP_024306539.1:p.Leu745= | |
| XM_024450772.1:c.1179G>C | XP_024306540.1:p.Leu393= | |
| NM_000263.4:c.2178G>C MANE Select | NP_000254.2:p.Leu726= |