HGVS | Genome Assembly |
---|---|
NC_000004.12:g.105542556C>T , CM000666.2:g.105542556C>T | GRCh38 |
NC_000004.11:g.106463713C>T , CM000666.1:g.106463713C>T | GRCh37 |
NC_000004.10:g.106683162C>T | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
XR_939038.1:n.449G>A | ||
XR_939039.1:n.609G>A | ||
XR_939040.1:n.296-1080G>A | ||
XR_001741410.1:n.464G>A | ||
XR_001741411.1:n.940G>A | ||
XR_001741412.1:n.449+15G>A | ||
XR_001741413.1:n.464G>A | ||
XR_001741414.1:n.449+15G>A | ||
XR_939038.2:n.464G>A | ||
XR_939040.2:n.311-1080G>A |