HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32443293G>C , CM000668.2:g.32443293G>C | GRCh38 |
NC_000006.11:g.32411070G>C , CM000668.1:g.32411070G>C | GRCh37 |
NC_000006.10:g.32519048G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000395388.7:c.437G>C MANE Select | ENSP00000378786.2:p.Trp146Ser | |
ENST00000374982.5:c.362G>C | ENSP00000364121.5:p.Trp121Ser | |
ENST00000395388.6:c.437G>C | ENSP00000378786.2:p.Trp146Ser | |
NM_019111.4:c.437G>C | NP_061984.2:p.Trp146Ser | |
NM_019111.5:c.437G>C MANE Select | NP_061984.2:p.Trp146Ser |