HGVS | Genome Assembly |
---|---|
NC_000022.11:g.19724260C>G , CM000684.2:g.19724260C>G | GRCh38 |
NC_000022.10:g.19711783C>G , CM000684.1:g.19711783C>G | GRCh37 |
NC_000022.9:g.18091783C>G | NCBI36 |
NG_007974.1:g.5718C>G , LRG_478:g.5718C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000366425.4:c.417C>G (GP1BB) MANE Select | ENSP00000383382.2:p.Ala139= | |
ENST00000366425.3:c.417C>G (GP1BB) | ENSP00000383382.2:p.Ala139= | |
ENST00000431044.5:c.*1502C>G (SEPTIN5) | ENSP00000399685.1:n.*1502C>G | |
NM_000407.4:c.417C>G , LRG_478t1:c.417C>G (GP1BB) | NP_000398.1:p.Ala139= | |
NR_037611.1:n.4157C>G | ||
NR_037612.1:n.2661C>G | ||
NM_000407.5:c.417C>G (GP1BB) MANE Select | NP_000398.1:p.Ala139= |