HGVS | Genome Assembly |
---|---|
NC_000003.12:g.184135360G>T , CM000665.2:g.184135360G>T | GRCh38 |
NC_000003.11:g.183853148G>T , CM000665.1:g.183853148G>T | GRCh37 |
NC_000003.10:g.185335842G>T | NCBI36 |
NG_015826.1:g.5339G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000471832.2:c.-26G>T | ENSP00000497786.1:n.-26G>T | |
ENST00000648314.1:c.-26G>T | ENSP00000496920.1:n.-26G>T | |
ENST00000648915.2:c.-26G>T MANE Select | ENSP00000497160.1:n.-26G>T | |
ENST00000649814.1:n.24G>T | ||
ENST00000273783.7:c.-26G>T | ENSP00000273783.3:n.-26G>T | |
ENST00000491144.5:n.323G>T | ||
NM_003907.2:c.-26G>T | NP_003898.2:n.-26G>T | |
XR_924208.1:n.926G>T | ||
NM_003907.3:c.-26G>T MANE Select | NP_003898.2:n.-26G>T | |
XR_001740352.2:n.338G>T | ||
XR_001740353.2:n.338G>T | ||
XR_924208.2:n.338G>T |