HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652509C>G , CM000663.2:g.171652509C>G | GRCh38 |
NC_000001.10:g.171621649C>G , CM000663.1:g.171621649C>G | GRCh37 |
NC_000001.9:g.169888272C>G | NCBI36 |
NG_008859.1:g.5125G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.103G>C MANE Select | ENSP00000037502.5:p.Ala35Pro | |
ENST00000638471.1:c.103G>C | ENSP00000491206.1:p.Ala35Pro | |
ENST00000037502.10:c.103G>C | ENSP00000037502.5:p.Ala35Pro | |
ENST00000614688.1:c.103G>C | ENSP00000478680.1:p.Ala35Pro | |
NM_000261.1:c.103G>C | NP_000252.1:p.Ala35Pro | |
NM_000261.2:c.103G>C MANE Select | NP_000252.1:p.Ala35Pro |