HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47283764A>G , CM000679.2:g.47283764A>G | GRCh38 |
NC_000017.10:g.45361130A>G , CM000679.1:g.45361130A>G | GRCh37 |
NC_000017.9:g.42716129A>G | NCBI36 |
NG_008332.2:g.34923A>G , LRG_481:g.34923A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696963.1:c.361+215A>G | ENSP00000513002.1:n.361+215A>G | |
ENST00000559488.7:c.361+215A>G MANE Select | ENSP00000452786.2:n.361+215A>G | |
ENST00000559488.5:c.361+215A>G | ENSP00000452786.1:n.361+215A>G | |
ENST00000560629.1:c.326+215A>G | ||
ENST00000571680.1:c.361+215A>G | ENSP00000461626.1:n.361+215A>G | |
NM_000212.2:c.361+215A>G , LRG_481t1:c.361+215A>G | NP_000203.2:n.361+215A>G | |
NM_000212.3:c.361+215A>G MANE Select | NP_000203.2:n.361+215A>G |