HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186265950C>A , CM000666.2:g.186265950C>A | GRCh38 |
NC_000004.11:g.187187104C>A , CM000666.1:g.187187104C>A | GRCh37 |
NC_000004.10:g.187424098C>A | NCBI36 |
NG_008051.1:g.4987C>A , LRG_583:g.4987C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000403665.6:c.-347C>A | ENSP00000384957.2:n.-347C>A | |
XM_005262821.2:c.-347C>A | XP_005262878.1:n.-347C>A | |
XM_005262822.2:c.-347C>A | XP_005262879.1:n.-347C>A | |
XM_005262823.2:c.-347C>A | XP_005262880.1:n.-347C>A | |
XM_005262824.1:c.-347C>A | XP_005262881.1:n.-347C>A | |
XM_006714137.1:c.-347C>A | XP_006714200.1:n.-347C>A | |
XR_938706.1:n.6C>A | ||
XR_938707.1:n.6C>A |