HGVS | Genome Assembly |
---|---|
NC_000006.12:g.96057416G>A , CM000668.2:g.96057416G>A | GRCh38 |
NC_000006.11:g.96505292G>A , CM000668.1:g.96505292G>A | GRCh37 |
NC_000006.10:g.96612013G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000302103.6:c.-98+41204G>A MANE Select | ENSP00000302599.4:n.-98+41204G>A | |
ENST00000302103.5:c.-98+41204G>A | ENSP00000302599.4:n.-98+41204G>A | |
NM_006581.3:c.-98+41204G>A | NP_006572.2:n.-98+41204G>A | |
XM_011535384.1:c.-98+36443G>A | XP_011533686.1:n.-98+36443G>A | |
XM_017010190.1:c.-215+41204G>A | XP_016865679.1:n.-215+41204G>A | |
XR_001744267.2:n.1842C>T | ||
NM_006581.4:c.-98+41204G>A MANE Select | NP_006572.2:n.-98+41204G>A |