HGVS | Genome Assembly |
---|---|
NC_000023.11:g.101348550T>A , CM000685.2:g.101348550T>A | GRCh38 |
NC_000023.10:g.100603538T>A , CM000685.1:g.100603538T>A | GRCh37 |
NC_000023.9:g.100490194T>A | NCBI36 |
NG_009616.1:g.42675A>T , LRG_128:g.42675A>T | |
NG_011734.1:g.5420A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372902.4:c.115A>T MANE Select | ENSP00000361993.3:p.Met39Leu | |
ENST00000644112.2:c.115A>T | ENSP00000494385.1:p.Met39Leu | |
ENST00000645279.1:c.115A>T | ENSP00000494239.1:p.Met39Leu | |
ENST00000647480.1:n.26A>T | ||
ENST00000372902.3:c.115A>T | ENSP00000361993.3:p.Met39Leu | |
ENST00000480575.1:n.200A>T | ||
NM_001145951.1:c.115A>T | NP_001139423.1:p.Met39Leu | |
NM_004085.3:c.115A>T | NP_004076.1:p.Met39Leu | |
NM_004085.4:c.115A>T MANE Select | NP_004076.1:p.Met39Leu | |
NM_001145951.2:c.115A>T | NP_001139423.1:p.Met39Leu |