HGVS | Genome Assembly |
---|---|
NC_000023.11:g.37728031A>C , CM000685.2:g.37728031A>C | GRCh38 |
NC_000023.10:g.37587284A>C , CM000685.1:g.37587284A>C | GRCh37 |
NC_000023.9:g.37472223A>C | NCBI36 |
NG_007473.1:g.47172A>C | |
NG_007473.3:g.47152A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378616.5:c.904A>C MANE Select | ENSP00000367879.3:p.Ile302Leu | |
ENST00000378616.3:c.904A>C | ENSP00000367879.3:p.Ile302Leu | |
ENST00000465127.1:c.171+302031A>C | ENSP00000417050.1:n.171+302031A>C | |
NM_021083.2:c.904A>C | NP_066569.1:p.Ile302Leu | |
NM_021083.4:c.904A>C MANE Select | NP_066569.1:p.Ile302Leu |