HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21010905T>C , CM000664.2:g.21010905T>C | GRCh38 |
NC_000002.11:g.21233777T>C , CM000664.1:g.21233777T>C | GRCh37 |
NC_000002.10:g.21087282T>C | NCBI36 |
NG_011793.1:g.38169A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000233242.5:c.5963A>G MANE Select | ENSP00000233242.1:p.Asn1988Ser | |
ENST00000616098.4:c.5963A>G | ENSP00000477990.1:p.Asn1988Ser | |
NM_000384.2:c.5963A>G | NP_000375.2:p.Asn1988Ser | |
XM_011532809.1:c.5864+99A>G | XP_011531111.1:n.5864+99A>G | |
NM_000384.3:c.5963A>G MANE Select | NP_000375.3:p.Asn1988Ser |