HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586529C>T , CM000673.2:g.67586529C>T | GRCh38 |
NC_000011.9:g.67354000C>T , CM000673.1:g.67354000C>T | GRCh37 |
NC_000011.8:g.67110576C>T | NCBI36 |
NG_012075.1:g.7935C>T , LRG_723:g.7935C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.477C>T | ENSP00000381604.1:p.Ala159= | |
ENST00000398606.10:c.585C>T MANE Select | ENSP00000381607.3:p.Ala195= | |
ENST00000398603.5:c.477C>T | ENSP00000381604.1:p.Ala159= | |
ENST00000398606.7:c.585C>T | ENSP00000381607.3:p.Ala195= | |
ENST00000467591.1:n.696C>T | ||
ENST00000494593.1:n.1557C>T | ||
ENST00000498765.5:c.648C>T | ||
NM_000852.3:c.585C>T , LRG_723t1:c.585C>T | NP_000843.1:p.Ala195= | |
NM_000852.4:c.585C>T MANE Select | NP_000843.1:p.Ala195= |