HGVS | Genome Assembly |
---|---|
NC_000005.10:g.128300917G>A , CM000667.2:g.128300917G>A | GRCh38 |
NC_000005.9:g.127636609G>A , CM000667.1:g.127636609G>A | GRCh37 |
NC_000005.8:g.127664508G>A | NCBI36 |
NG_008750.1:g.242127C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000703783.1:n.2850C>T | ||
ENST00000703785.1:n.2769C>T | ||
ENST00000262464.9:c.6066C>T MANE Select | ENSP00000262464.4:p.Ala2022= | |
ENST00000262464.8:c.6066C>T | ENSP00000262464.4:p.Ala2022= | |
ENST00000508053.5:c.6066C>T | ENSP00000424571.1:p.Ala2022= | |
ENST00000619499.4:c.6063C>T | ENSP00000482132.1:p.Ala2021= | |
NM_001999.3:c.6066C>T | NP_001990.2:p.Ala2022= | |
XM_017009228.2:c.5913C>T | XP_016864717.1:p.Ala1971= | |
NM_001999.4:c.6066C>T MANE Select | NP_001990.2:p.Ala2022= |