HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625343A>C , CM000673.2:g.22625343A>C | GRCh38 |
NC_000011.9:g.22646889A>C , CM000673.1:g.22646889A>C | GRCh37 |
NC_000011.8:g.22603465A>C | NCBI36 |
NG_007425.1:g.5499T>G , LRG_527:g.5499T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.468T>G MANE Select | ENSP00000330875.3:p.Asn156Lys | |
ENST00000327470.4:c.468T>G | ENSP00000330875.3:p.Asn156Lys | |
NM_022725.3:c.468T>G , LRG_527t1:c.468T>G | NP_073562.1:p.Asn156Lys | |
NM_022725.4:c.468T>G MANE Select | NP_073562.1:p.Asn156Lys |