HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5227030T>G , CM000673.2:g.5227030T>G | GRCh38 |
NC_000011.9:g.5248260T>G , CM000673.1:g.5248260T>G | GRCh37 |
NC_000011.8:g.5204836T>G | NCBI36 |
NG_000007.3:g.70586A>C | |
NG_059281.1:g.5042A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647020.1:c.-9A>C | ENSP00000494175.1:n.-9A>C | |
ENST00000335295.4:c.-9A>C MANE Select | ENSP00000333994.3:n.-9A>C | |
ENST00000380315.2:c.-9A>C | ENSP00000369671.2:n.-9A>C | |
ENST00000485743.1:n.43A>C | ||
ENST00000633227.1:c.-9A>C | ENSP00000488004.1:n.-9A>C | |
NM_000518.4:c.-9A>C | NP_000509.1:n.-9A>C | |
NM_000518.5:c.-9A>C MANE Select | NP_000509.1:n.-9A>C |