HGVS | Genome Assembly |
---|---|
NC_000002.12:g.96143257G= , CM000664.2:g.96143257G= | GRCh38 |
NC_000002.11:g.96808996G= , CM000664.1:g.96808996G= | GRCh37 |
NC_000002.10:g.96172723G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000288943.5:c.*566C= MANE Select | ENSP00000288943.4:n.*566C= | |
ENST00000288943.4:c.*566C= | ENSP00000288943.4:n.*566C= | |
NM_004418.3:c.*566C= | NP_004409.1:n.*566C= | |
XM_017003546.1:c.*566C= | XP_016859035.1:n.*566C= | |
NM_004418.4:c.*566C= MANE Select | NP_004409.1:n.*566C= |