HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240877485T= , CM000664.2:g.240877485T= | GRCh38 |
NC_000002.11:g.241816902T= , CM000664.1:g.241816902T= | GRCh37 |
NC_000002.10:g.241465575T= | NCBI36 |
NG_008005.1:g.13741T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.847-52T= MANE Select | ENSP00000302620.3:n.847-52T= | |
ENST00000307503.3:c.847-52T= | ENSP00000302620.3:n.847-52T= | |
ENST00000470255.1:n.573T= | ||
NM_000030.2:c.847-52T= | NP_000021.1:n.847-52T= | |
NM_000030.3:c.847-52T= MANE Select | NP_000021.1:n.847-52T= |