HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94942198T>C , CM000672.2:g.94942198T>C | GRCh38 |
NC_000010.10:g.96701955T>C , CM000672.1:g.96701955T>C | GRCh37 |
NC_000010.9:g.96691945T>C | NCBI36 |
NG_008385.1:g.8541T>C | |
NG_008385.2:g.9041T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.338T>C MANE Select | ENSP00000260682.6:p.Val113Ala | |
ENST00000643112.1:c.338T>C | ENSP00000496202.1:p.Val113Ala | |
ENST00000645207.1:n.491T>C | ||
ENST00000260682.6:c.338T>C | ENSP00000260682.6:p.Val113Ala | |
ENST00000461906.1:n.363T>C | ||
ENST00000473496.1:n.109T>C | ||
NM_000771.3:c.338T>C | NP_000762.2:p.Val113Ala | |
NM_000771.4:c.338T>C MANE Select | NP_000762.2:p.Val113Ala |