HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104034106C>A , CM000672.2:g.104034106C>A | GRCh38 |
NC_000010.10:g.105793864C>A , CM000672.1:g.105793864C>A | GRCh37 |
NC_000010.9:g.105783854C>A | NCBI36 |
NG_007069.1:g.56775G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.3749G>T | ENSP00000358748.3:p.Gly1250Val | |
ENST00000647647.1:c.25G>T | ||
ENST00000648076.2:c.3995G>T MANE Select | ENSP00000497653.1:p.Gly1332Val | |
ENST00000353479.9:c.3995G>T | ENSP00000340937.5:p.Gly1332Val | |
ENST00000369733.7:c.3749G>T | ENSP00000358748.3:p.Gly1250Val | |
NM_000494.3:c.3995G>T | NP_000485.3:p.Gly1332Val | |
NM_000494.4:c.3995G>T MANE Select | NP_000485.3:p.Gly1332Val |