HGVS | Genome Assembly |
---|---|
NC_000007.14:g.73682967C>G , CM000669.2:g.73682967C>G | GRCh38 |
NC_000007.13:g.73097297C>G , CM000669.1:g.73097297C>G | GRCh37 |
NC_000007.12:g.72735233C>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395176.3:c.457G>C MANE Select | ENSP00000378605.1:p.Ala153Pro | |
ENST00000395176.2:c.457G>C | ENSP00000378605.1:p.Ala153Pro | |
NM_032317.2:c.457G>C | NP_115693.2:p.Ala153Pro | |
NM_032317.3:c.457G>C MANE Select | NP_115693.2:p.Ala153Pro |