HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48476808C= , CM000675.2:g.48476808C= | GRCh38 |
NC_000013.10:g.49050944C= , CM000675.1:g.49050944C= | GRCh37 |
NC_000013.9:g.47948945C= | NCBI36 |
NG_009009.1:g.178062C= , LRG_517:g.178062C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.2628C= MANE Select | ENSP00000267163.4:p.Arg876= | |
ENST00000643064.1:c.194+95365C= | ||
ENST00000650461.1:c.2628C= | ENSP00000497193.1:p.Arg876= | |
ENST00000267163.4:c.2628C= | ENSP00000267163.4:p.Arg876= | |
ENST00000484879.1:n.362C= | ||
ENST00000531171.5:n.231C= | ||
NM_000321.2:c.2628C= , LRG_517t1:c.2628C= | NP_000312.2:p.Arg876= | |
XM_011535171.1:c.2367C= | XP_011533473.1:p.Arg789= | |
XM_011535171.2:c.2367C= | XP_011533473.1:p.Arg789= | |
NM_000321.3:c.2628C= MANE Select | NP_000312.2:p.Arg876= |