HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21007398C>G , CM000664.2:g.21007398C>G | GRCh38 |
NC_000002.11:g.21230270C>G , CM000664.1:g.21230270C>G | GRCh37 |
NC_000002.10:g.21083775C>G | NCBI36 |
NG_011793.1:g.41676G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000233242.5:c.9470G>C MANE Select | ENSP00000233242.1:p.Gly3157Ala | |
ENST00000616098.4:c.9470G>C | ENSP00000477990.1:p.Gly3157Ala | |
NM_000384.2:c.9470G>C | NP_000375.2:p.Gly3157Ala | |
XM_011532809.1:c.5869+3335G>C | XP_011531111.1:n.5869+3335G>C | |
NM_000384.3:c.9470G>C MANE Select | NP_000375.3:p.Gly3157Ala |