HGVS | Genome Assembly |
---|---|
NC_000002.12:g.84425588G>C , CM000664.2:g.84425588G>C | GRCh38 |
NC_000002.11:g.84652712G>C , CM000664.1:g.84652712G>C | GRCh37 |
NC_000002.10:g.84506223G>C | NCBI36 |
NG_016755.1:g.38875C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000393868.7:c.841C>G MANE Select | ENSP00000377446.2:p.Pro281Ala | |
ENST00000651342.1:c.*281C>G | ENSP00000498471.1:n.*281C>G | |
ENST00000393868.6:c.841C>G | ENSP00000377446.2:p.Pro281Ala | |
ENST00000484365.1:n.1349C>G | ||
ENST00000487809.1:n.588C>G | ||
ENST00000491123.5:n.687C>G | ||
NM_003849.3:c.841C>G | NP_003840.2:p.Pro281Ala | |
NM_003849.4:c.841C>G MANE Select | NP_003840.2:p.Pro281Ala |