HGVS | Genome Assembly |
---|---|
NC_000019.10:g.6713210C>G , CM000681.2:g.6713210C>G | GRCh38 |
NC_000019.9:g.6713221C>G , CM000681.1:g.6713221C>G | GRCh37 |
NC_000019.8:g.6664221C>G | NCBI36 |
NG_009557.1:g.12442G>C , LRG_27:g.12442G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000695652.1:c.859G>C | ENSP00000512083.1:p.Ala287Pro | |
ENST00000695654.1:c.106G>C | ENSP00000512085.1:p.Ala36Pro | |
ENST00000695692.1:n.306G>C | ||
ENST00000245907.11:c.982G>C MANE Select | ENSP00000245907.4:p.Ala328Pro | |
ENST00000245907.10:c.982G>C | ENSP00000245907.4:p.Ala328Pro | |
ENST00000594270.5:n.106G>C | ||
ENST00000595577.1:n.486G>C | ||
ENST00000597442.5:n.232G>C | ||
NM_000064.3:c.982G>C | NP_000055.2:p.Ala328Pro | |
NM_000064.4:c.982G>C MANE Select | NP_000055.2:p.Ala328Pro |