HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48476724A>T , CM000675.2:g.48476724A>T | GRCh38 |
NC_000013.10:g.49050860A>T , CM000675.1:g.49050860A>T | GRCh37 |
NC_000013.9:g.47948861A>T | NCBI36 |
NG_009009.1:g.177978A>T , LRG_517:g.177978A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.2544A>T MANE Select | ENSP00000267163.4:p.Ile848= | |
ENST00000643064.1:c.194+95281A>T | ||
ENST00000650461.1:c.2544A>T | ENSP00000497193.1:p.Ile848= | |
ENST00000267163.4:c.2544A>T | ENSP00000267163.4:p.Ile848= | |
ENST00000484879.1:n.278A>T | ||
ENST00000531171.5:n.147A>T | ||
NM_000321.2:c.2544A>T , LRG_517t1:c.2544A>T | NP_000312.2:p.Ile848= | |
XM_011535171.1:c.2283A>T | XP_011533473.1:p.Ile761= | |
XM_011535171.2:c.2283A>T | XP_011533473.1:p.Ile761= | |
NM_000321.3:c.2544A>T MANE Select | NP_000312.2:p.Ile848= |