HGVS | Genome Assembly |
---|---|
NC_000001.11:g.196995723T>C , CM000663.2:g.196995723T>C | GRCh38 |
NC_000001.10:g.196964853T>C , CM000663.1:g.196964853T>C | GRCh37 |
NC_000001.9:g.195231476T>C | NCBI36 |
NG_016365.1:g.23187T>C , LRG_227:g.23187T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000699466.1:c.359T>C | ENSP00000514393.1:p.Val120Ala | |
ENST00000699467.1:n.683T>C | ||
ENST00000699468.1:c.-24-391T>C | ENSP00000514394.1:n.-24-391T>C | |
ENST00000256785.5:c.614T>C MANE Select | ENSP00000256785.4:p.Val205Ala | |
ENST00000256785.4:c.614T>C | ENSP00000256785.4:p.Val205Ala | |
NM_030787.3:c.614T>C , LRG_227t1:c.614T>C | NP_110414.1:p.Val205Ala | |
XM_011510020.1:c.623T>C | XP_011508322.1:p.Val208Ala | |
XM_011510020.2:c.623T>C | XP_011508322.1:p.Val208Ala | |
NM_030787.4:c.614T>C MANE Select | NP_110414.1:p.Val205Ala |