HGVS | Genome Assembly |
---|---|
NC_000004.12:g.163324692C= , CM000666.2:g.163324692C= | GRCh38 |
NC_000004.11:g.164245844C= , CM000666.1:g.164245844C= | GRCh37 |
NC_000004.10:g.164465294C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000296533.3:c.*611G= MANE Select | ENSP00000354652.2:n.*611G= | |
ENST00000296533.2:c.*611G= | ENSP00000354652.2:n.*611G= | |
NM_000909.5:c.*611G= | NP_000900.1:n.*611G= | |
XM_005263031.2:c.*611G= | XP_005263088.1:n.*611G= | |
XM_011532010.1:c.*611G= | XP_011530312.1:n.*611G= | |
XM_005263031.4:c.*611G= | XP_005263088.1:n.*611G= | |
XM_011532010.3:c.*611G= | XP_011530312.1:n.*611G= | |
NM_000909.6:c.*611G= MANE Select | NP_000900.1:n.*611G= |