HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154993104C>A , CM000685.2:g.154993104C>A | GRCh38 |
NC_000023.10:g.154221379C>A , CM000685.1:g.154221379C>A | GRCh37 |
NC_000023.9:g.153874573C>A | NCBI36 |
NG_011403.1:g.34620G>T | |
NG_011403.2:g.34620G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.433G>T MANE Select | ENSP00000353393.4:p.Asp145Tyr | |
ENST00000647125.1:c.*219G>T | ENSP00000496062.1:n.*219G>T | |
ENST00000360256.8:c.433G>T | ENSP00000353393.4:p.Asp145Tyr | |
ENST00000423959.5:c.328G>T | ENSP00000409446.1:p.Asp110Tyr | |
ENST00000453950.1:c.415G>T | ENSP00000389153.1:p.Asp139Tyr | |
NM_000132.3:c.433G>T | NP_000123.1:p.Asp145Tyr | |
XM_011531126.1:c.328G>T | XP_011529428.1:p.Asp110Tyr | |
NM_000132.4:c.433G>T MANE Select | NP_000123.1:p.Asp145Tyr |