HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154863106T= , CM000685.2:g.154863106T= | GRCh38 |
NC_000023.10:g.154091381T= , CM000685.1:g.154091381T= | GRCh37 |
NC_000023.9:g.153744575T= | NCBI36 |
NG_011403.1:g.164618A= | |
NG_011403.2:g.164618A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.6551A= MANE Select | ENSP00000353393.4:p.Glu2184= | |
ENST00000644698.1:c.284A= | ENSP00000495706.1:p.Glu95= | |
ENST00000330287.10:c.146A= | ENSP00000327895.6:p.Glu49= | |
ENST00000360256.8:c.6551A= | ENSP00000353393.4:p.Glu2184= | |
NM_000132.3:c.6551A= | NP_000123.1:p.Glu2184= | |
NM_019863.2:c.146A= | NP_063916.1:p.Glu49= | |
XM_011531126.1:c.6446A= | XP_011529428.1:p.Glu2149= | |
NM_000132.4:c.6551A= MANE Select | NP_000123.1:p.Glu2184= | |
NM_019863.3:c.146A= | NP_063916.1:p.Glu49= |