HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94021027A>C , CM000663.2:g.94021027A>C | GRCh38 |
NC_000001.10:g.94486583A>C , CM000663.1:g.94486583A>C | GRCh37 |
NC_000001.9:g.94259171A>C | NCBI36 |
NG_009073.1:g.105123T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.5018+213T>G MANE Select | ENSP00000359245.3:n.5018+213T>G | |
ENST00000370225.3:c.5018+213T>G | ENSP00000359245.3:n.5018+213T>G | |
ENST00000460514.1:n.512+213T>G | ||
ENST00000470771.1:n.128+213T>G | ||
ENST00000536513.5:c.1394+213T>G | ENSP00000439707.2:n.1394+213T>G | |
NM_000350.2:c.5018+213T>G | NP_000341.2:n.5018+213T>G | |
NM_000350.3:c.5018+213T>G MANE Select | NP_000341.2:n.5018+213T>G |