HGVS | Genome Assembly |
---|---|
NC_000016.10:g.88727057G= , CM000678.2:g.88727057G= | GRCh38 |
NC_000016.9:g.88793465G= , CM000678.1:g.88793465G= | GRCh37 |
NC_000016.8:g.87320966G= | NCBI36 |
NG_042229.1:g.63164C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000301015.14:c.3437C= MANE Select | ENSP00000301015.9:p.Pro1146= | |
ENST00000491917.2:n.423C= | ||
ENST00000301015.13:c.3437C= | ENSP00000301015.9:p.Pro1146= | |
NM_001142864.2:c.3437C= | NP_001136336.2:p.Pro1146= | |
NM_001142864.3:c.3437C= | NP_001136336.2:p.Pro1146= | |
NM_001142864.4:c.3437C= MANE Select | NP_001136336.2:p.Pro1146= |