HGVS | Genome Assembly |
---|---|
NC_000012.12:g.71943058G>T , CM000674.2:g.71943058G>T | GRCh38 |
NC_000012.11:g.72336838G>T , CM000674.1:g.72336838G>T | GRCh37 |
NC_000012.10:g.70623105G>T | NCBI36 |
NG_008279.1:g.9213G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000333850.4:c.256-1236G>T MANE Select | ENSP00000329093.3:n.256-1236G>T | |
ENST00000333850.3:c.256-1236G>T | ENSP00000329093.3:n.256-1236G>T | |
ENST00000546576.1:n.266-1236G>T | ||
NM_173353.3:c.256-1236G>T | NP_775489.2:n.256-1236G>T | |
XR_245894.2:n.356-1236G>T | ||
XR_001748575.1:n.356-1236G>T | ||
NM_173353.4:c.256-1236G>T MANE Select | NP_775489.2:n.256-1236G>T |