HGVS | Genome Assembly |
---|---|
NC_000005.10:g.44305613A>G , CM000667.2:g.44305613A>G | GRCh38 |
NC_000005.9:g.44305715A>G , CM000667.1:g.44305715A>G | GRCh37 |
NC_000005.8:g.44341472A>G | NCBI36 |
NG_011446.1:g.88070T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264664.5:c.430-421T>C MANE Select | ENSP00000264664.4:n.430-421T>C | |
ENST00000264664.4:c.430-421T>C | ENSP00000264664.4:n.430-421T>C | |
NM_004465.1:c.430-421T>C | NP_004456.1:n.430-421T>C | |
XM_005248264.2:c.430-421T>C | XP_005248321.1:n.430-421T>C | |
XM_005248264.4:c.430-421T>C | XP_005248321.1:n.430-421T>C | |
NM_004465.2:c.430-421T>C MANE Select | NP_004456.1:n.430-421T>C |