HGVS | Genome Assembly |
---|---|
NC_000019.10:g.41353053C>A , CM000681.2:g.41353053C>A | GRCh38 |
NC_000019.9:g.41858958C>A , CM000681.1:g.41858958C>A | GRCh37 |
NC_000019.8:g.46550798C>A | NCBI36 |
NG_013091.1:g.16121G>T | |
NG_013364.1:g.5874G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221930.6:c.-9G>T (TGFB1) MANE Select | ENSP00000221930.4:n.-9G>T | |
ENST00000221930.5:c.-9G>T (TGFB1) | ENSP00000221930.4:n.-9G>T | |
ENST00000539627.5:c.-30+1851C>A (TMEM91) | ENSP00000441900.1:n.-30+1851C>A | |
ENST00000604424.1:n.350+1851C>A | ||
NM_000660.5:c.-9G>T (TGFB1) | NP_000651.3:n.-9G>T | |
XM_011527242.1:c.-9G>T (TGFB1) | XP_011525544.1:n.-9G>T | |
NM_000660.6:c.-9G>T (TGFB1) | NP_000651.3:n.-9G>T | |
XM_011527242.2:c.-9G>T (TGFB1) | XP_011525544.1:n.-9G>T | |
NM_000660.7:c.-9G>T (TGFB1) MANE Select | NP_000651.3:n.-9G>T |