HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23424035T>C , CM000676.2:g.23424035T>C | GRCh38 |
NC_000014.8:g.23893244T>C , CM000676.1:g.23893244T>C | GRCh37 |
NC_000014.7:g.22963084T>C | NCBI36 |
NG_007884.1:g.16627A>G , LRG_384:g.16627A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.2794A>G MANE Select | ENSP00000347507.3:p.Met932Val | |
ENST00000355349.3:c.2794A>G | ENSP00000347507.3:p.Met932Val | |
NM_000257.3:c.2794A>G | NP_000248.2:p.Met932Val | |
XR_245686.3:n.2900A>G | ||
XM_017021340.1:c.2794A>G | XP_016876829.1:p.Met932Val | |
NM_000257.4:c.2794A>G MANE Select | NP_000248.2:p.Met932Val |