HGVS | Genome Assembly |
---|---|
NC_000006.12:g.38682872A>C , CM000668.2:g.38682872A>C | GRCh38 |
NC_000006.11:g.38650648A>C , CM000668.1:g.38650648A>C | GRCh37 |
NC_000006.10:g.38758626A>C | NCBI36 |
NG_012074.1:g.25305T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373365.5:c.312T>G MANE Select | ENSP00000362463.3:p.Asn104Lys | |
ENST00000373365.4:c.312T>G | ENSP00000362463.3:p.Asn104Lys | |
ENST00000470973.1:n.344T>G | ||
NM_006708.2:c.312T>G | NP_006699.2:p.Asn104Lys | |
NM_006708.3:c.312T>G MANE Select | NP_006699.2:p.Asn104Lys |