HGVS | Genome Assembly |
---|---|
NC_000008.11:g.23682818C>G , CM000670.2:g.23682818C>G | GRCh38 |
NC_000008.10:g.23540331C>G , CM000670.1:g.23540331C>G | GRCh37 |
NC_000008.9:g.23596276C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380871.5:c.72G>C MANE Select | ENSP00000370253.4:p.Lys24Asn | |
ENST00000380871.4:c.72G>C | ENSP00000370253.4:p.Lys24Asn | |
ENST00000523261.1:c.33+39G>C | ENSP00000429729.1:n.33+39G>C | |
NM_001256339.1:c.33+39G>C | NP_001243268.1:n.33+39G>C | |
NM_006167.3:c.72G>C | NP_006158.2:p.Lys24Asn | |
NR_046072.1:n.18+86G>C | ||
XR_001745842.1:n.1312+14068C>G | ||
NM_006167.4:c.72G>C MANE Select | NP_006158.2:p.Lys24Asn | |
NR_046072.2:n.35+86G>C |