HGVS | Genome Assembly |
---|---|
NC_000014.9:g.91272677G>A , CM000676.2:g.91272677G>A | GRCh38 |
NC_000014.8:g.91739021G>A , CM000676.1:g.91739021G>A | GRCh37 |
NC_000014.7:g.90808774G>A | NCBI36 |
NG_033118.1:g.150168C>T | |
NG_033118.2:g.150168C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389857.11:c.6035C>T MANE Select | ENSP00000374507.6:p.Pro2012Leu | |
ENST00000331194.8:c.1469C>T | ENSP00000330332.8:p.Pro490Leu | |
ENST00000389857.10:c.6035C>T | ENSP00000374507.6:p.Pro2012Leu | |
ENST00000556726.5:c.2263C>T | ||
NM_001080414.3:c.6035C>T | NP_001073883.2:p.Pro2012Leu | |
XM_011536796.1:c.5927C>T | XP_011535098.1:p.Pro1976Leu | |
XM_011536796.2:c.5927C>T | XP_011535098.1:p.Pro1976Leu | |
XM_017021336.1:c.3116C>T | XP_016876825.1:p.Pro1039Leu | |
NM_001080414.4:c.6035C>T MANE Select | NP_001073883.2:p.Pro2012Leu |