HGVS | Genome Assembly |
---|---|
NC_000014.9:g.91272754G= , CM000676.2:g.91272754G= | GRCh38 |
NC_000014.8:g.91739098G= , CM000676.1:g.91739098G= | GRCh37 |
NC_000014.7:g.90808851G= | NCBI36 |
NG_033118.1:g.150091C= | |
NG_033118.2:g.150091C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000389857.11:c.5958C= MANE Select | ENSP00000374507.6:p.Pro1986= | |
ENST00000331194.8:c.1392C= | ENSP00000330332.8:p.Pro464= | |
ENST00000389857.10:c.5958C= | ENSP00000374507.6:p.Pro1986= | |
ENST00000556726.5:c.2186C= | ||
NM_001080414.3:c.5958C= | NP_001073883.2:p.Pro1986= | |
XM_011536796.1:c.5850C= | XP_011535098.1:p.Pro1950= | |
XM_011536796.2:c.5850C= | XP_011535098.1:p.Pro1950= | |
XM_017021336.1:c.3039C= | XP_016876825.1:p.Pro1013= | |
NM_001080414.4:c.5958C= MANE Select | NP_001073883.2:p.Pro1986= |