HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55044012T= , CM000663.2:g.55044012T= | GRCh38 |
NC_000001.10:g.55509685T= , CM000663.1:g.55509685T= | GRCh37 |
NC_000001.9:g.55282273T= | NCBI36 |
NG_009061.1:g.9466T= , LRG_275:g.9466T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.377T= | ENSP00000501161.2:p.Met126= | |
ENST00000710286.1:c.734T= | ENSP00000518176.1:p.Met245= | |
ENST00000673662.1:n.47T= | ||
ENST00000673726.1:c.377T= | ENSP00000501004.1:p.Met126= | |
ENST00000673903.1:c.2T= | ENSP00000501257.1:p.Met1= | |
ENST00000302118.5:c.377T= MANE Select | ENSP00000303208.5:p.Met126= | |
NM_174936.3:c.377T= , LRG_275t1:c.377T= | NP_777596.2:p.Met126= | |
NR_110451.1:n.182+3609T= | ||
NM_174936.4:c.377T= MANE Select | NP_777596.2:p.Met126= | |
NR_110451.2:n.182+3609T= |