HGVS | Genome Assembly |
---|---|
NC_000023.11:g.101348622C>G , CM000685.2:g.101348622C>G | GRCh38 |
NC_000023.10:g.100603610C>G , CM000685.1:g.100603610C>G | GRCh37 |
NC_000023.9:g.100490266C>G | NCBI36 |
NG_009616.1:g.42603G>C , LRG_128:g.42603G>C | |
NG_011734.1:g.5348G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372902.4:c.43G>C MANE Select | ENSP00000361993.3:p.Val15Leu | |
ENST00000644112.2:c.43G>C | ENSP00000494385.1:p.Val15Leu | |
ENST00000645279.1:c.43G>C | ENSP00000494239.1:p.Val15Leu | |
ENST00000372902.3:c.43G>C | ENSP00000361993.3:p.Val15Leu | |
ENST00000480575.1:n.128G>C | ||
NM_001145951.1:c.43G>C | NP_001139423.1:p.Val15Leu | |
NM_004085.3:c.43G>C | NP_004076.1:p.Val15Leu | |
NM_004085.4:c.43G>C MANE Select | NP_004076.1:p.Val15Leu | |
NM_001145951.2:c.43G>C | NP_001139423.1:p.Val15Leu |