HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57765931A= , CM000674.2:g.57765931A= | GRCh38 |
NC_000012.11:g.58159714A= , CM000674.1:g.58159714A= | GRCh37 |
NC_000012.10:g.56445981A= | NCBI36 |
NG_007076.1:g.6263T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000546609.2:n.298+76T= | ||
ENST00000713544.1:c.386+76T= | ENSP00000518840.1:n.386+76T= | |
ENST00000713545.1:c.386+76T= | ENSP00000518841.1:n.386+76T= | |
ENST00000228606.9:c.386+76T= MANE Select | ENSP00000228606.4:n.386+76T= | |
ENST00000228606.8:c.386+76T= | ENSP00000228606.4:n.386+76T= | |
ENST00000546496.1:n.214+76T= | ||
ENST00000546609.1:c.298+76T= | ||
ENST00000547344.5:n.440+76T= | ||
ENST00000552186.1:n.505+76T= | ||
NM_000785.3:c.386+76T= | NP_000776.1:n.386+76T= | |
NM_000785.4:c.386+76T= MANE Select | NP_000776.1:n.386+76T= |