Linked Data
MyVariant Identifiers:
chr5:g.80503100G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.81207281G>A , CM000667.2:g.81207281G>A | GRCh38 |
| NC_000005.9:g.80503100G>A , CM000667.1:g.80503100G>A | GRCh37 |
| NC_000005.8:g.80538856G>A | NCBI36 |
| NG_030334.1:g.251593G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265080.9:c.3003G>A MANE Select | ENSP00000265080.4:p.Leu1001= | |
| ENST00000265080.8:c.3003G>A | ENSP00000265080.4:p.Leu1001= | |
| ENST00000503795.1:c.3003G>A | ENSP00000421771.1:p.Leu1001= | |
| NM_006909.2:c.3003G>A | NP_008840.1:p.Leu1001= | |
| XM_017009682.2:c.2718G>A | XP_016865171.1:p.Leu906= | |
| XR_002956166.1:n.3119G>A | ||
| NM_006909.3:c.3003G>A MANE Select | NP_008840.1:p.Leu1001= |