HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1416108T>G , CM000667.2:g.1416108T>G | GRCh38 |
NC_000005.9:g.1416223T>G , CM000667.1:g.1416223T>G | GRCh37 |
NC_000005.8:g.1469223T>G | NCBI36 |
NG_015885.1:g.34321A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000270349.12:c.1021A>C MANE Select | ENSP00000270349.9:p.Asn341His | |
ENST00000270349.11:c.1021A>C | ENSP00000270349.9:p.Asn341His | |
ENST00000511750.1:n.471A>C | ||
NM_001044.4:c.1021A>C | NP_001035.1:p.Asn341His | |
NM_001044.5:c.1021A>C MANE Select | NP_001035.1:p.Asn341His |