HGVS | Genome Assembly |
---|---|
NC_000011.10:g.19548084T= , CM000673.2:g.19548084T= | GRCh38 |
NC_000011.9:g.19569631T= , CM000673.1:g.19569631T= | GRCh37 |
NC_000011.8:g.19526207T= | NCBI36 |
NG_030347.1:g.202361T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360655.8:c.75+197057T= | ENSP00000353871.4:n.75+197057T= | |
NM_001111018.1:c.75+197057T= | NP_001104488.1:n.75+197057T= | |
XM_011520452.1:c.75+197057T= | XP_011518754.1:n.75+197057T= | |
XM_011520452.2:c.75+197057T= | XP_011518754.1:n.75+197057T= | |
XM_017018520.2:c.75+197057T= | XP_016874009.1:n.75+197057T= | |
XM_017018522.1:c.75+197057T= | XP_016874011.1:n.75+197057T= | |
XM_024448758.1:c.75+197057T= | XP_024304526.1:n.75+197057T= | |
NM_001111018.2:c.75+197057T= | NP_001104488.1:n.75+197057T= |