HGVS | Genome Assembly |
---|---|
NC_000012.12:g.102846906T>G , CM000674.2:g.102846906T>G | GRCh38 |
NC_000012.11:g.103240684T>G , CM000674.1:g.103240684T>G | GRCh37 |
NC_000012.10:g.101764814T>G | NCBI36 |
NG_008690.1:g.75697A>C | |
NG_008690.2:g.116505A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000553106.6:c.958A>C MANE Select | ENSP00000448059.1:p.Lys320Gln | |
ENST00000307000.7:c.943A>C | ENSP00000303500.2:p.Lys315Gln | |
ENST00000549247.6:n.717A>C | ||
ENST00000551114.2:n.620A>C | ||
ENST00000553106.5:c.958A>C | ENSP00000448059.1:p.Lys320Gln | |
ENST00000635477.1:c.74-2475A>C | ||
ENST00000635528.1:n.473A>C | ||
NM_000277.1:c.958A>C | NP_000268.1:p.Lys320Gln | |
XM_011538422.1:c.913-2475A>C | XP_011536724.1:n.913-2475A>C | |
NM_000277.2:c.958A>C | NP_000268.1:p.Lys320Gln | |
NM_001354304.1:c.958A>C | NP_001341233.1:p.Lys320Gln | |
NM_000277.3:c.958A>C MANE Select | NP_000268.1:p.Lys320Gln | |
NM_001354304.2:c.958A>C | NP_001341233.1:p.Lys320Gln |