HGVS | Genome Assembly |
---|---|
NC_000019.10:g.15540738A= , CM000681.2:g.15540738A= | GRCh38 |
NC_000019.9:g.15651549A= , CM000681.1:g.15651549A= | GRCh37 |
NC_000019.8:g.15512549A= | NCBI36 |
NG_007987.1:g.37214A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269703.8:c.939+21A= MANE Select | ENSP00000269703.1:n.939+21A= | |
ENST00000269703.7:c.939+21A= | ENSP00000269703.1:n.939+21A= | |
ENST00000601005.2:c.939+21A= | ENSP00000469866.1:n.939+21A= | |
NM_173483.3:c.939+21A= | NP_775754.2:n.939+21A= | |
XM_011527692.1:c.939+21A= | XP_011525994.1:n.939+21A= | |
XM_011527693.1:c.939+21A= | XP_011525995.1:n.939+21A= | |
XM_011527692.2:c.939+21A= | XP_011525994.1:n.939+21A= | |
XM_011527693.2:c.939+21A= | XP_011525995.1:n.939+21A= | |
NM_173483.4:c.939+21A= MANE Select | NP_775754.2:n.939+21A= |