HGVS | Genome Assembly |
---|---|
NC_000007.14:g.117479801A>C , CM000669.2:g.117479801A>C | GRCh38 |
NC_000007.13:g.117119855A>C , CM000669.1:g.117119855A>C | GRCh37 |
NC_000007.12:g.116907091A>C | NCBI36 |
NG_016465.4:g.19018A>C , LRG_663:g.19018A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000446805.2:c.-191+107A>C | ENSP00000417012.1:n.-191+107A>C | |
ENST00000673785.1:c.-406+13970A>C | ENSP00000501235.1:n.-406+13970A>C | |
ENST00000446805.1:c.-191+107A>C | ENSP00000417012.1:n.-191+107A>C | |
ENST00000546407.1:n.166+3993A>C | ||
XM_011515751.1:c.143+456A>C | XP_011514053.1:n.143+456A>C | |
XM_011515752.1:c.143+456A>C | XP_011514054.1:n.143+456A>C | |
XM_011515753.1:c.-191+107A>C | XP_011514055.1:n.-191+107A>C | |
XM_011515754.1:c.-519+107A>C | XP_011514056.1:n.-519+107A>C |