HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1416109G>T , CM000667.2:g.1416109G>T | GRCh38 |
NC_000005.9:g.1416224G>T , CM000667.1:g.1416224G>T | GRCh37 |
NC_000005.8:g.1469224G>T | NCBI36 |
NG_015885.1:g.34320C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.1020C>A MANE Select | ENSP00000270349.9:p.Asn340Lys | |
ENST00000270349.11:c.1020C>A | ENSP00000270349.9:p.Asn340Lys | |
ENST00000511750.1:n.470C>A | ||
NM_001044.4:c.1020C>A | NP_001035.1:p.Asn340Lys | |
NM_001044.5:c.1020C>A MANE Select | NP_001035.1:p.Asn340Lys |