HGVS | Genome Assembly |
---|---|
NC_000022.11:g.19724050G>T , CM000684.2:g.19724050G>T | GRCh38 |
NC_000022.10:g.19711573G>T , CM000684.1:g.19711573G>T | GRCh37 |
NC_000022.9:g.18091573G>T | NCBI36 |
NG_007974.1:g.5508G>T , LRG_478:g.5508G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366425.4:c.207G>T (GP1BB) MANE Select | ENSP00000383382.2:p.Ala69= | |
ENST00000366425.3:c.207G>T (GP1BB) | ENSP00000383382.2:p.Ala69= | |
ENST00000431044.5:c.*1292G>T (SEPTIN5) | ENSP00000399685.1:n.*1292G>T | |
ENST00000455843.5:c.*1292G>T (SEPTIN5) | ENSP00000391731.1:n.*1292G>T | |
ENST00000470814.1:n.2179G>T (SEPTIN5) | ||
NM_000407.4:c.207G>T , LRG_478t1:c.207G>T (GP1BB) | NP_000398.1:p.Ala69= | |
NR_037611.1:n.3947G>T | ||
NR_037612.1:n.2451G>T | ||
NM_000407.5:c.207G>T (GP1BB) MANE Select | NP_000398.1:p.Ala69= |