HGVS | Genome Assembly |
---|---|
NC_000001.11:g.169485561A= , CM000663.2:g.169485561A= | GRCh38 |
NC_000001.10:g.169454799A= , CM000663.1:g.169454799A= | GRCh37 |
NC_000001.9:g.167721423A= | NCBI36 |
NG_008255.1:g.5410T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000236137.10:c.204+2T= MANE Select | ENSP00000236137.5:n.204+2T= | |
ENST00000646596.1:c.204+2T= | ENSP00000494404.1:n.204+2T= | |
ENST00000236137.9:c.204+2T= | ENSP00000236137.5:n.204+2T= | |
ENST00000367804.4:c.204+2T= | ENSP00000356778.3:n.204+2T= | |
NM_006996.2:c.204+2T= | NP_008927.1:n.204+2T= | |
XM_011509076.1:c.12+492T= | XP_011507378.1:n.12+492T= | |
XM_011509077.1:c.204+2T= | XP_011507379.1:n.204+2T= | |
NM_001319667.1:c.204+2T= | NP_001306596.1:n.204+2T= | |
NM_006996.3:c.204+2T= MANE Select | NP_008927.1:n.204+2T= |