HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19954158G>C , CM000670.2:g.19954158G>C | GRCh38 |
NC_000008.10:g.19811669G>C , CM000670.1:g.19811669G>C | GRCh37 |
NC_000008.9:g.19855949G>C | NCBI36 |
NG_008855.1:g.20088G>C | |
NG_008855.2:g.57442G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.580G>C MANE Select | ENSP00000497642.1:p.Ala194Pro | |
ENST00000311322.8:c.580G>C | ENSP00000309757.6:p.Ala194Pro | |
NM_000237.2:c.580G>C | NP_000228.1:p.Ala194Pro | |
NM_000237.3:c.580G>C MANE Select | NP_000228.1:p.Ala194Pro |