HGVS | Genome Assembly |
---|---|
NC_000007.14:g.74789318G= , CM000669.2:g.74789318G= | GRCh38 |
NC_000007.13:g.74203662G= , CM000669.1:g.74203662G= | GRCh37 |
NC_000007.12:g.73841598G= | NCBI36 |
NG_009078.2:g.20355G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000289473.10:c.*158G= | ENSP00000289473.4:n.*158G= | |
NM_000265.5:c.*158G= | NP_000256.4:n.*158G= | |
XM_005250543.3:c.*252G= | XP_005250600.2:n.*252G= | |
XM_011516498.1:c.*205G= | XP_011514800.1:n.*205G= | |
XM_011516501.1:c.*158G= | XP_011514803.1:n.*158G= | |
NM_000265.6:c.*158G= | NP_000256.4:n.*158G= |