HGVS | Genome Assembly |
---|---|
NC_000002.12:g.232966240G>A , CM000664.2:g.232966240G>A | GRCh38 |
NC_000002.11:g.233830950G>A , CM000664.1:g.233830950G>A | GRCh37 |
NC_000002.10:g.233539194G>A | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264051.8:c.383+3974C>T MANE Select | ENSP00000264051.3:n.383+3974C>T | |
ENST00000264051.7:c.383+3974C>T | ENSP00000264051.3:n.383+3974C>T | |
NM_019850.2:c.383+3974C>T | NP_062824.2:n.383+3974C>T | |
XM_011510923.1:c.383+3974C>T | XP_011509225.1:n.383+3974C>T | |
XM_011510923.3:c.383+3974C>T | XP_011509225.1:n.383+3974C>T | |
NM_019850.3:c.383+3974C>T MANE Select | NP_062824.2:n.383+3974C>T |