HGVS | Genome Assembly |
---|---|
NC_000019.10:g.48966348A>G , CM000681.2:g.48966348A>G | GRCh38 |
NC_000019.9:g.49469605A>G , CM000681.1:g.49469605A>G | GRCh37 |
NC_000019.8:g.54161417A>G | NCBI36 |
NG_008152.1:g.6040A>G | |
NG_012923.1:g.32006T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331825.11:c.317A>G MANE Select | ENSP00000366525.2:p.Lys106Arg | |
ENST00000331825.10:c.317A>G | ENSP00000366525.2:p.Lys106Arg | |
ENST00000622577.2:c.317A>G | ENSP00000484043.1:p.Lys106Arg | |
NM_000146.3:c.317A>G | NP_000137.2:p.Lys106Arg | |
XM_024451447.1:c.827A>G | XP_024307215.1:p.Lys276Arg | |
NM_000146.4:c.317A>G MANE Select | NP_000137.2:p.Lys106Arg |