HGVS | Genome Assembly |
---|---|
NC_000022.11:g.19724149C= , CM000684.2:g.19724149C= | GRCh38 |
NC_000022.10:g.19711672C= , CM000684.1:g.19711672C= | GRCh37 |
NC_000022.9:g.18091672C= | NCBI36 |
NG_007974.1:g.5607C= , LRG_478:g.5607C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000366425.4:c.306C= (GP1BB) MANE Select | ENSP00000383382.2:p.Ala102= | |
ENST00000366425.3:c.306C= (GP1BB) | ENSP00000383382.2:p.Ala102= | |
ENST00000431044.5:c.*1391C= (SEPTIN5) | ENSP00000399685.1:n.*1391C= | |
ENST00000455843.5:c.*1391C= (SEPTIN5) | ENSP00000391731.1:n.*1391C= | |
ENST00000470814.1:n.2278C= (SEPTIN5) | ||
NM_000407.4:c.306C= , LRG_478t1:c.306C= (GP1BB) | NP_000398.1:p.Ala102= | |
NR_037611.1:n.4046C= | ||
NR_037612.1:n.2550C= | ||
NM_000407.5:c.306C= (GP1BB) MANE Select | NP_000398.1:p.Ala102= |