HGVS | Genome Assembly |
---|---|
NC_000006.12:g.18130736C>T , CM000668.2:g.18130736C>T | GRCh38 |
NC_000006.11:g.18130967C>T , CM000668.1:g.18130967C>T | GRCh37 |
NC_000006.10:g.18238946C>T | NCBI36 |
NG_012137.2:g.29408G>A | |
NG_012137.3:g.29408G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309983.5:c.670G>A MANE Select | ENSP00000312304.4:p.Glu224Lys | |
ENST00000309983.4:c.670G>A | ENSP00000312304.4:p.Glu224Lys | |
NM_000367.3:c.670G>A | NP_000358.1:p.Glu224Lys | |
XM_011514839.1:c.625G>A | XP_011513141.1:p.Glu209Lys | |
XM_011514840.1:c.601G>A | XP_011513142.1:p.Glu201Lys | |
NM_000367.4:c.670G>A | NP_000358.1:p.Glu224Lys | |
NM_001346817.1:c.670G>A | NP_001333746.1:p.Glu224Lys | |
NM_001346818.1:c.625G>A | NP_001333747.1:p.Glu209Lys | |
NM_000367.5:c.670G>A MANE Select | NP_000358.1:p.Glu224Lys |