HGVS | Genome Assembly |
---|---|
NC_000022.11:g.19724142T>A , CM000684.2:g.19724142T>A | GRCh38 |
NC_000022.10:g.19711665T>A , CM000684.1:g.19711665T>A | GRCh37 |
NC_000022.9:g.18091665T>A | NCBI36 |
NG_007974.1:g.5600T>A , LRG_478:g.5600T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000366425.4:c.299T>A (GP1BB) MANE Select | ENSP00000383382.2:p.Leu100Gln | |
ENST00000366425.3:c.299T>A (GP1BB) | ENSP00000383382.2:p.Leu100Gln | |
ENST00000431044.5:c.*1384T>A (SEPTIN5) | ENSP00000399685.1:n.*1384T>A | |
ENST00000455843.5:c.*1384T>A (SEPTIN5) | ENSP00000391731.1:n.*1384T>A | |
ENST00000470814.1:n.2271T>A (SEPTIN5) | ||
NM_000407.4:c.299T>A , LRG_478t1:c.299T>A (GP1BB) | NP_000398.1:p.Leu100Gln | |
NR_037611.1:n.4039T>A | ||
NR_037612.1:n.2543T>A | ||
NM_000407.5:c.299T>A (GP1BB) MANE Select | NP_000398.1:p.Leu100Gln |