HGVS | Genome Assembly |
---|---|
NC_000014.9:g.91272727G>A , CM000676.2:g.91272727G>A | GRCh38 |
NC_000014.8:g.91739071G>A , CM000676.1:g.91739071G>A | GRCh37 |
NC_000014.7:g.90808824G>A | NCBI36 |
NG_033118.1:g.150118C>T | |
NG_033118.2:g.150118C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389857.11:c.5985C>T MANE Select | ENSP00000374507.6:p.Ala1995= | |
ENST00000331194.8:c.1419C>T | ENSP00000330332.8:p.Ala473= | |
ENST00000389857.10:c.5985C>T | ENSP00000374507.6:p.Ala1995= | |
ENST00000556726.5:c.2213C>T | ||
NM_001080414.3:c.5985C>T | NP_001073883.2:p.Ala1995= | |
XM_011536796.1:c.5877C>T | XP_011535098.1:p.Ala1959= | |
XM_011536796.2:c.5877C>T | XP_011535098.1:p.Ala1959= | |
XM_017021336.1:c.3066C>T | XP_016876825.1:p.Ala1022= | |
NM_001080414.4:c.5985C>T MANE Select | NP_001073883.2:p.Ala1995= |