HGVS | Genome Assembly |
---|---|
NC_000011.10:g.19548387A>G , CM000673.2:g.19548387A>G | GRCh38 |
NC_000011.9:g.19569934A>G , CM000673.1:g.19569934A>G | GRCh37 |
NC_000011.8:g.19526510A>G | NCBI36 |
NG_030347.1:g.202664A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360655.8:c.75+197360A>G | ENSP00000353871.4:n.75+197360A>G | |
NM_001111018.1:c.75+197360A>G | NP_001104488.1:n.75+197360A>G | |
XM_011520452.1:c.75+197360A>G | XP_011518754.1:n.75+197360A>G | |
XM_011520452.2:c.75+197360A>G | XP_011518754.1:n.75+197360A>G | |
XM_017018520.2:c.75+197360A>G | XP_016874009.1:n.75+197360A>G | |
XM_017018522.1:c.75+197360A>G | XP_016874011.1:n.75+197360A>G | |
XM_024448758.1:c.75+197360A>G | XP_024304526.1:n.75+197360A>G | |
NM_001111018.2:c.75+197360A>G | NP_001104488.1:n.75+197360A>G |