HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159320332G>T , CM000667.2:g.159320332G>T | GRCh38 |
NC_000005.9:g.158747340G>T , CM000667.1:g.158747340G>T | GRCh37 |
NC_000005.8:g.158679918G>T | NCBI36 |
NG_009618.1:g.15142C>A , LRG_71:g.15142C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.41C>A | ENSP00000512849.1:p.Thr14Asn | |
ENST00000696751.1:c.*166C>A | ENSP00000512850.1:n.*166C>A | |
ENST00000231228.3:c.671C>A MANE Select | ENSP00000231228.2:p.Thr224Asn | |
ENST00000231228.2:c.671C>A | ENSP00000231228.2:p.Thr224Asn | |
NM_002187.2:c.671C>A , LRG_71t1:c.671C>A | NP_002178.2:p.Thr224Asn | |
NM_002187.3:c.671C>A MANE Select | NP_002178.2:p.Thr224Asn |