HGVS | Genome Assembly |
---|---|
NC_000002.12:g.44942218_44942219insAGCGGC , CM000664.2:g.44942218_44942219insAGCGGC | GRCh38 |
NC_000002.11:g.45169357_45169358insAGCGGC , CM000664.1:g.45169357_45169358insAGCGGC | GRCh37 |
NC_000002.10:g.45022861_45022862insAGCGGC | NCBI36 |
NG_016222.1:g.5321_5322insAGCGGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260653.5:c.114_115insAGCGGC MANE Select | ENSP00000260653.3:p.Ala38_Gly39insSerGly | |
ENST00000260653.4:c.114_115insAGCGGC | ENSP00000260653.3:p.Ala38_Gly39insSerGly | |
NM_005413.3:c.114_115insAGCGGC | NP_005404.1:p.Ala38_Gly39insSerGly | |
XM_011533042.1:c.114_115insAGCGGC | XP_011531344.1:p.Ala38_Gly39insSerGly | |
NM_005413.4:c.114_115insAGCGGC MANE Select | NP_005404.1:p.Ala38_Gly39insSerGly |