HGVS | Genome Assembly |
---|---|
NC_000008.11:g.118947794A= , CM000670.2:g.118947794A= | GRCh38 |
NC_000008.10:g.119960033A= , CM000670.1:g.119960033A= | GRCh37 |
NC_000008.9:g.120029214A= | NCBI36 |
NG_012202.1:g.9351T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297350.9:c.30+3998T= MANE Select | ENSP00000297350.4:n.30+3998T= | |
ENST00000297350.8:c.30+3998T= | ENSP00000297350.4:n.30+3998T= | |
ENST00000517352.1:c.30+3998T= | ENSP00000427924.1:n.30+3998T= | |
NM_002546.3:c.30+3998T= | NP_002537.3:n.30+3998T= | |
NM_002546.4:c.30+3998T= MANE Select | NP_002537.3:n.30+3998T= |