HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15180084_15180085delinsGC , CM000681.2:g.15180084_15180085delinsGC | GRCh38 |
NC_000019.9:g.15290895_15290896delinsGC , CM000681.1:g.15290895_15290896delinsGC | GRCh37 |
NC_000019.8:g.15151895_15151896delinsGC | NCBI36 |
NG_009819.1:g.25897_25898delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263388.7:c.3314_3315delinsGC MANE Select | ENSP00000263388.1:p.Gly1105= | |
ENST00000263388.6:c.3314_3315delinsGC | ENSP00000263388.1:p.Gly1105= | |
ENST00000601011.1:c.3155_3156delinsGC | ENSP00000473138.1:p.Gly1052= | |
NM_000435.2:c.3314_3315delinsGC | NP_000426.2:p.Gly1105= | |
XM_005259924.3:c.3158_3159delinsGC | XP_005259981.1:p.Gly1053= | |
XM_005259924.4:c.3158_3159delinsGC | XP_005259981.1:p.Gly1053= | |
NM_000435.3:c.3314_3315delinsGC MANE Select | NP_000426.2:p.Gly1105= |