HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186680320G= , CM000663.2:g.186680320G= | GRCh38 |
NC_000001.10:g.186649452G= , CM000663.1:g.186649452G= | GRCh37 |
NC_000001.9:g.184916075G= | NCBI36 |
NG_028206.2:g.5108C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367468.10:c.-30C= MANE Select | ENSP00000356438.5:n.-30C= | |
ENST00000680451.1:c.-30C= | ENSP00000506242.1:n.-30C= | |
ENST00000681605.1:c.-30C= | ENSP00000504900.1:n.-30C= | |
ENST00000367468.9:c.-30C= | ENSP00000356438.5:n.-30C= | |
ENST00000490885.6:n.104C= | ||
ENST00000559800.1:n.104C= | ||
NM_000963.3:c.-30C= | NP_000954.1:n.-30C= | |
NM_000963.4:c.-30C= MANE Select | NP_000954.1:n.-30C= |