HGVS | Genome Assembly |
---|---|
NC_000005.10:g.150848439A>C , CM000667.2:g.150848439A>C | GRCh38 |
NC_000005.9:g.150228001A>C , CM000667.1:g.150228001A>C | GRCh37 |
NC_000005.8:g.150208194A>C | NCBI36 |
NG_027809.1:g.6917A>C | |
NG_027809.2:g.6917A>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000522154.2:c.316A>C MANE Select | ENSP00000428220.1:p.Met106Leu | |
ENST00000522154.1:c.316A>C | ENSP00000428220.1:p.Met106Leu | |
NM_001145805.1:c.316A>C | NP_001139277.1:p.Met106Leu | |
XM_011537641.1:c.316A>C | XP_011535943.1:p.Met106Leu | |
NM_001346557.1:c.316A>C | NP_001333486.1:p.Met106Leu | |
NM_001346557.2:c.316A>C | NP_001333486.1:p.Met106Leu | |
NM_001145805.2:c.316A>C MANE Select | NP_001139277.1:p.Met106Leu | |
NR_170598.1:n.1431A>C |