HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21174684G>T , CM000674.2:g.21174684G>T | GRCh38 |
NC_000012.11:g.21327618G>T , CM000674.1:g.21327618G>T | GRCh37 |
NC_000012.10:g.21218885G>T | NCBI36 |
NG_011745.1:g.48491G>T , LRG_1022:g.48491G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.334G>T MANE Select | ENSP00000256958.2:p.Ala112Ser | |
ENST00000256958.2:c.334G>T | ENSP00000256958.2:p.Ala112Ser | |
ENST00000543498.5:c.426-2092G>T | ||
NM_006446.4:c.334G>T , LRG_1022t1:c.334G>T | NP_006437.3:p.Ala112Ser | |
NM_006446.5:c.334G>T MANE Select | NP_006437.3:p.Ala112Ser |