HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625017C>T , CM000673.2:g.22625017C>T | GRCh38 |
NC_000011.9:g.22646563C>T , CM000673.1:g.22646563C>T | GRCh37 |
NC_000011.8:g.22603139C>T | NCBI36 |
NG_007425.1:g.5825G>A , LRG_527:g.5825G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.794G>A MANE Select | ENSP00000330875.3:p.Ser265Asn | |
ENST00000327470.4:c.794G>A | ENSP00000330875.3:p.Ser265Asn | |
NM_022725.3:c.794G>A , LRG_527t1:c.794G>A | NP_073562.1:p.Ser265Asn | |
NM_022725.4:c.794G>A MANE Select | NP_073562.1:p.Ser265Asn |