HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240877571C= , CM000664.2:g.240877571C= | GRCh38 |
NC_000002.11:g.241816988C= , CM000664.1:g.241816988C= | GRCh37 |
NC_000002.10:g.241465661C= | NCBI36 |
NG_008005.1:g.13827C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.881C= MANE Select | ENSP00000302620.3:p.Ala294= | |
ENST00000307503.3:c.881C= | ENSP00000302620.3:p.Ala294= | |
ENST00000470255.1:n.659C= | ||
NM_000030.2:c.881C= | NP_000021.1:p.Ala294= | |
NM_000030.3:c.881C= MANE Select | NP_000021.1:p.Ala294= |