HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154903968C>T , CM000685.2:g.154903968C>T | GRCh38 |
NC_000023.10:g.154132243C>T , CM000685.1:g.154132243C>T | GRCh37 |
NC_000023.9:g.153785437C>T | NCBI36 |
NG_011403.1:g.123756G>A | |
NG_011403.2:g.123756G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5936G>A MANE Select | ENSP00000353393.4:p.Gly1979Glu | |
ENST00000360256.8:c.5936G>A | ENSP00000353393.4:p.Gly1979Glu | |
NM_000132.3:c.5936G>A | NP_000123.1:p.Gly1979Glu | |
XM_011531126.1:c.5831G>A | XP_011529428.1:p.Gly1944Glu | |
NM_000132.4:c.5936G>A MANE Select | NP_000123.1:p.Gly1979Glu |