HGVS | Genome Assembly |
---|---|
NC_000019.10:g.45803896G>A , CM000681.2:g.45803896G>A | GRCh38 |
NC_000019.9:g.46307154G>A , CM000681.1:g.46307154G>A | GRCh37 |
NC_000019.8:g.50998994G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221538.8:c.1653+356C>T MANE Select | ENSP00000221538.2:n.1653+356C>T | |
ENST00000221538.7:c.1653+356C>T | ENSP00000221538.2:n.1653+356C>T | |
ENST00000597055.1:c.1653+356C>T | ENSP00000472630.1:n.1653+356C>T | |
ENST00000600188.5:c.861+356C>T | ENSP00000471559.1:n.861+356C>T | |
NM_030785.3:c.1653+356C>T | NP_110412.1:n.1653+356C>T | |
XM_011527351.1:c.1653+356C>T | XP_011525653.1:n.1653+356C>T | |
XM_011527351.2:c.1653+356C>T | XP_011525653.1:n.1653+356C>T | |
NM_030785.4:c.1653+356C>T MANE Select | NP_110412.1:n.1653+356C>T |