HGVS | Genome Assembly |
---|---|
NC_000009.12:g.114796471G= , CM000671.2:g.114796471G= | GRCh38 |
NC_000009.11:g.117558751G= , CM000671.1:g.117558751G= | GRCh37 |
NC_000009.10:g.116598572G= | NCBI36 |
NG_011488.2:g.14658C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374045.5:c.211-2903C= MANE Select | ENSP00000363157.3:n.211-2903C= | |
ENST00000374045.4:c.211-2903C= | ENSP00000363157.3:n.211-2903C= | |
NM_005118.3:c.211-2903C= | NP_005109.2:n.211-2903C= | |
NM_005118.4:c.211-2903C= MANE Select | NP_005109.2:n.211-2903C= |