HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119414288C= , CM000665.2:g.119414288C= | GRCh38 |
NC_000003.11:g.119133135C= , CM000665.1:g.119133135C= | GRCh37 |
NC_000003.10:g.120615825C= | NCBI36 |
NG_007665.2:g.124916C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264245.9:c.2359C= MANE Select | ENSP00000264245.4:p.Pro787= | |
ENST00000264245.8:c.2359C= | ENSP00000264245.4:p.Pro787= | |
NM_020754.3:c.2359C= | NP_065805.2:p.Pro787= | |
XM_005247671.3:c.2266C= | XP_005247728.1:p.Pro756= | |
XM_006713714.2:c.2299C= | XP_006713777.1:p.Pro767= | |
XM_006713714.3:c.2299C= | XP_006713777.1:p.Pro767= | |
XM_017006955.1:c.1867C= | XP_016862444.1:p.Pro623= | |
NM_020754.4:c.2359C= MANE Select | NP_065805.2:p.Pro787= |