HGVS | Genome Assembly |
---|---|
NC_000006.12:g.98874273T= , CM000668.2:g.98874273T= | GRCh38 |
NC_000006.11:g.99322149T= , CM000668.1:g.99322149T= | GRCh37 |
NC_000006.10:g.99428870T= | NCBI36 |
NG_033903.1:g.78734A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369244.7:c.*5A= MANE Select | ENSP00000358247.1:n.*5A= | |
ENST00000229971.2:c.*5A= | ENSP00000229971.1:n.*5A= | |
ENST00000369244.6:c.*5A= | ENSP00000358247.1:n.*5A= | |
NM_001278716.1:c.*5A= | NP_001265645.1:n.*5A= | |
NM_012160.4:c.*5A= | NP_036292.2:n.*5A= | |
NR_103836.1:n.1916A= | ||
XM_005266930.1:c.*5A= | XP_005266987.1:n.*5A= | |
XM_005266930.3:c.*5A= | XP_005266987.1:n.*5A= | |
XM_017010726.1:c.*5A= | XP_016866215.1:n.*5A= | |
XM_017010727.2:c.*5A= | XP_016866216.1:n.*5A= | |
XM_017010728.1:c.*5A= | XP_016866217.1:n.*5A= | |
NM_001278716.2:c.*5A= MANE Select | NP_001265645.1:n.*5A= | |
NR_103836.2:n.1856A= | ||
NM_012160.5:c.*5A= | NP_036292.2:n.*5A= |