HGVS | Genome Assembly |
---|---|
NC_000003.12:g.119413881T>C , CM000665.2:g.119413881T>C | GRCh38 |
NC_000003.11:g.119132728T>C , CM000665.1:g.119132728T>C | GRCh37 |
NC_000003.10:g.120615418T>C | NCBI36 |
NG_007665.2:g.124509T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264245.9:c.1952T>C MANE Select | ENSP00000264245.4:p.Leu651Pro | |
ENST00000264245.8:c.1952T>C | ENSP00000264245.4:p.Leu651Pro | |
NM_020754.3:c.1952T>C | NP_065805.2:p.Leu651Pro | |
XM_005247671.3:c.1859T>C | XP_005247728.1:p.Leu620Pro | |
XM_006713714.2:c.1892T>C | XP_006713777.1:p.Leu631Pro | |
XM_006713714.3:c.1892T>C | XP_006713777.1:p.Leu631Pro | |
XM_017006955.1:c.1460T>C | XP_016862444.1:p.Leu487Pro | |
NM_020754.4:c.1952T>C MANE Select | NP_065805.2:p.Leu651Pro |