HGVS | Genome Assembly |
---|---|
NC_000012.12:g.109573582T= , CM000674.2:g.109573582T= | GRCh38 |
NC_000012.11:g.110011387T= , CM000674.1:g.110011387T= | GRCh37 |
NC_000012.10:g.108495770T= | NCBI36 |
NG_007096.1:g.4916A= | |
NG_007702.1:g.4888T= , LRG_156:g.4888T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000546277.6:c.-15+11T= (MVK) | ENSP00000438153.2:n.-15+11T= | |
ENST00000535044.1:n.231+11T= (MVK) | ||
ENST00000539335.5:c.-6+11T= (MVK) | ENSP00000440379.1:n.-6+11T= | |
ENST00000545712.6:c.-102A= (MMAB) | ENSP00000445920.1:n.-102A= | |
ENST00000546277.5:c.-15+11T= (MVK) | ENSP00000438153.1:n.-15+11T= | |
XM_011538372.1:c.-15+11T= (MVK) | XP_011536674.1:n.-15+11T= | |
XM_017019313.2:c.-15+11T= (MVK) | XP_016874802.1:n.-15+11T= | |
XM_024448982.1:c.-15+11T= (MVK) | XP_024304750.1:n.-15+11T= |