HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12812691T= , CM000686.2:g.12812691T= | GRCh38 |
NC_000024.9:g.14924626T= , CM000686.1:g.14924626T= | GRCh37 |
NC_000024.8:g.13434020T= | NCBI36 |
NG_008311.1:g.116467T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651177.1:c.4387-139T= | ENSP00000498372.1:n.4387-139T= | |
ENST00000338981.7:c.4387-139T= MANE Select | ENSP00000342812.3:n.4387-139T= | |
ENST00000426564.6:n.4399-139T= | ||
NM_004654.3:c.4387-139T= | NP_004645.2:n.4387-139T= | |
XM_011531469.1:c.4387-139T= | XP_011529771.1:n.4387-139T= | |
XM_011531470.1:c.4153-139T= | XP_011529772.1:n.4153-139T= | |
XM_017030078.2:c.4402-139T= | XP_016885567.1:n.4402-139T= | |
NM_004654.4:c.4387-139T= MANE Select | NP_004645.2:n.4387-139T= |