HGVS | Genome Assembly |
---|---|
NC_000006.12:g.18143639G>A , CM000668.2:g.18143639G>A | GRCh38 |
NC_000006.11:g.18143870G>A , CM000668.1:g.18143870G>A | GRCh37 |
NC_000006.10:g.18251849G>A | NCBI36 |
NG_012137.2:g.16505C>T | |
NG_012137.3:g.16505C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000309983.5:c.323C>T MANE Select | ENSP00000312304.4:p.Ser108Leu | |
ENST00000309983.4:c.323C>T | ENSP00000312304.4:p.Ser108Leu | |
NM_000367.3:c.323C>T | NP_000358.1:p.Ser108Leu | |
XM_011514839.1:c.323C>T | XP_011513141.1:p.Ser108Leu | |
XM_011514840.1:c.254C>T | XP_011513142.1:p.Ser85Leu | |
NM_000367.4:c.323C>T | NP_000358.1:p.Ser108Leu | |
NM_001346817.1:c.323C>T | NP_001333746.1:p.Ser108Leu | |
NM_001346818.1:c.323C>T | NP_001333747.1:p.Ser108Leu | |
NM_000367.5:c.323C>T MANE Select | NP_000358.1:p.Ser108Leu |