HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15540448A>G , CM000681.2:g.15540448A>G | GRCh38 |
NC_000019.9:g.15651259A>G , CM000681.1:g.15651259A>G | GRCh37 |
NC_000019.8:g.15512259A>G | NCBI36 |
NG_007987.1:g.36924A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269703.8:c.672-2A>G MANE Select | ENSP00000269703.1:n.672-2A>G | |
ENST00000269703.7:c.672-2A>G | ENSP00000269703.1:n.672-2A>G | |
ENST00000601005.2:c.672-2A>G | ENSP00000469866.1:n.672-2A>G | |
NM_173483.3:c.672-2A>G | NP_775754.2:n.672-2A>G | |
XM_011527692.1:c.672-2A>G | XP_011525994.1:n.672-2A>G | |
XM_011527693.1:c.672-2A>G | XP_011525995.1:n.672-2A>G | |
XM_011527692.2:c.672-2A>G | XP_011525994.1:n.672-2A>G | |
XM_011527693.2:c.672-2A>G | XP_011525995.1:n.672-2A>G | |
NM_173483.4:c.672-2A>G MANE Select | NP_775754.2:n.672-2A>G |