HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154837613G>T , CM000685.2:g.154837613G>T | GRCh38 |
NC_000023.10:g.154065888G>T , CM000685.1:g.154065888G>T | GRCh37 |
NC_000023.9:g.153719082G>T | NCBI36 |
NG_011403.1:g.190111C>A | |
NG_033065.1:g.2050C>A | |
NG_011403.2:g.190111C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.7040C>A MANE Select | ENSP00000353393.4:p.Ala2347Glu | |
ENST00000644698.1:c.773C>A | ENSP00000495706.1:p.Ala258Glu | |
ENST00000330287.10:c.635C>A | ENSP00000327895.6:p.Ala212Glu | |
ENST00000360256.8:c.7040C>A | ENSP00000353393.4:p.Ala2347Glu | |
NM_000132.3:c.7040C>A | NP_000123.1:p.Ala2347Glu | |
NM_019863.2:c.635C>A | NP_063916.1:p.Ala212Glu | |
XM_011531126.1:c.6935C>A | XP_011529428.1:p.Ala2312Glu | |
NM_000132.4:c.7040C>A MANE Select | NP_000123.1:p.Ala2347Glu | |
NM_019863.3:c.635C>A | NP_063916.1:p.Ala212Glu |