HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15540442C>T , CM000681.2:g.15540442C>T | GRCh38 |
NC_000019.9:g.15651253C>T , CM000681.1:g.15651253C>T | GRCh37 |
NC_000019.8:g.15512253C>T | NCBI36 |
NG_007987.1:g.36918C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269703.8:c.672-8C>T MANE Select | ENSP00000269703.1:n.672-8C>T | |
ENST00000269703.7:c.672-8C>T | ENSP00000269703.1:n.672-8C>T | |
ENST00000601005.2:c.672-8C>T | ENSP00000469866.1:n.672-8C>T | |
NM_173483.3:c.672-8C>T | NP_775754.2:n.672-8C>T | |
XM_011527692.1:c.672-8C>T | XP_011525994.1:n.672-8C>T | |
XM_011527693.1:c.672-8C>T | XP_011525995.1:n.672-8C>T | |
XM_011527692.2:c.672-8C>T | XP_011525994.1:n.672-8C>T | |
XM_011527693.2:c.672-8C>T | XP_011525995.1:n.672-8C>T | |
NM_173483.4:c.672-8C>T MANE Select | NP_775754.2:n.672-8C>T |