HGVS | Genome Assembly |
---|---|
NC_000022.11:g.50221303C>G , CM000684.2:g.50221303C>G | GRCh38 |
NC_000022.10:g.50659732C>G , CM000684.1:g.50659732C>G | GRCh37 |
NC_000022.9:g.49001859C>G | NCBI36 |
NG_032160.1:g.28669G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000248846.10:c.3056G>C MANE Select | ENSP00000248846.5:p.Ser1019Thr | |
ENST00000248846.9:c.3056G>C | ENSP00000248846.5:p.Ser1019Thr | |
ENST00000439308.6:c.3056G>C | ENSP00000397387.2:p.Ser1019Thr | |
ENST00000491449.5:n.1363G>C | ||
ENST00000498611.5:n.3589G>C | ||
NM_020461.3:c.3056G>C | NP_065194.2:p.Ser1019Thr | |
XR_938347.1:n.3621G>C | ||
XR_938348.1:n.3049+725G>C | ||
XR_001755343.2:n.3625G>C | ||
XR_001755344.2:n.3625G>C | ||
XR_002958720.1:n.3053+725G>C | ||
XR_938347.2:n.3625G>C | ||
NM_020461.4:c.3056G>C MANE Select | NP_065194.3:p.Ser1019Thr |