HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55091855_55091856delinsTC , CM000666.2:g.55091855_55091856delinsTC | GRCh38 |
NC_000004.11:g.55958022_55958023delinsTC , CM000666.1:g.55958022_55958023delinsTC | GRCh37 |
NC_000004.10:g.55652779_55652780delinsTC | NCBI36 |
NG_012004.1:g.38740_38741delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.3069+761_3069+762delinsGA MANE Select | ENSP00000263923.4:n.3069+761_3069+762delinsGA | |
ENST00000647068.1:n.3082+761_3082+762delinsGA | ||
ENST00000263923.4:c.3069+761_3069+762delinsGA | ENSP00000263923.4:n.3069+761_3069+762delinsGA | |
NM_002253.2:c.3069+761_3069+762delinsGA | NP_002244.1:n.3069+761_3069+762delinsGA | |
NM_002253.3:c.3069+761_3069+762delinsGA | NP_002244.1:n.3069+761_3069+762delinsGA | |
NM_002253.4:c.3069+761_3069+762delinsGA MANE Select | NP_002244.1:n.3069+761_3069+762delinsGA |