HGVS | Genome Assembly |
---|---|
NC_000006.12:g.35500012G= , CM000668.2:g.35500012G= | GRCh38 |
NC_000006.11:g.35467789G= , CM000668.1:g.35467789G= | GRCh37 |
NC_000006.10:g.35575767G= | NCBI36 |
NG_009077.1:g.17859C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000229771.11:c.1464C= MANE Select | ENSP00000229771.6:p.Val488= | |
ENST00000229771.10:c.1464C= | ENSP00000229771.6:p.Val488= | |
ENST00000322263.8:c.1305C= | ENSP00000319414.4:p.Val435= | |
ENST00000614066.4:c.1458C= | ENSP00000477534.1:p.Val486= | |
NM_001289395.1:c.1305C= | NP_001276324.1:p.Val435= | |
NM_003322.4:c.1464C= | NP_003313.3:p.Val488= | |
NM_003322.5:c.1464C= | NP_003313.3:p.Val488= | |
NM_003322.6:c.1464C= MANE Select | NP_003313.3:p.Val488= | |
NM_001289395.2:c.1305C= | NP_001276324.1:p.Val435= |