HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65246125T= , CM000674.2:g.65246125T= | GRCh38 |
NC_000012.11:g.65639905T= , CM000674.1:g.65639905T= | GRCh37 |
NC_000012.10:g.63926172T= | NCBI36 |
NG_016210.1:g.81555T= | |
NG_016210.2:g.81555T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.2573-37T= MANE Select | ENSP00000308369.2:n.2573-37T= | |
ENST00000308330.2:c.2573-37T= | ENSP00000308369.2:n.2573-37T= | |
ENST00000539442.1:n.555-37T= | ||
ENST00000544506.1:n.293-37T= | ||
ENST00000545026.1:n.391-37T= | ||
NM_001167614.1:c.2570-37T= | NP_001161086.1:n.2570-37T= | |
NM_014319.4:c.2573-37T= | NP_055134.2:n.2573-37T= | |
NM_014319.5:c.2573-37T= MANE Select | NP_055134.2:n.2573-37T= | |
NM_001167614.2:c.2570-37T= | NP_001161086.1:n.2570-37T= |