HGVS | Genome Assembly |
---|---|
NC_000011.10:g.19547730T>C , CM000673.2:g.19547730T>C | GRCh38 |
NC_000011.9:g.19569277T>C , CM000673.1:g.19569277T>C | GRCh37 |
NC_000011.8:g.19525853T>C | NCBI36 |
NG_030347.1:g.202007T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360655.8:c.75+196703T>C | ENSP00000353871.4:n.75+196703T>C | |
NM_001111018.1:c.75+196703T>C | NP_001104488.1:n.75+196703T>C | |
XM_011520452.1:c.75+196703T>C | XP_011518754.1:n.75+196703T>C | |
XM_011520452.2:c.75+196703T>C | XP_011518754.1:n.75+196703T>C | |
XM_017018520.2:c.75+196703T>C | XP_016874009.1:n.75+196703T>C | |
XM_017018522.1:c.75+196703T>C | XP_016874011.1:n.75+196703T>C | |
XM_024448758.1:c.75+196703T>C | XP_024304526.1:n.75+196703T>C | |
NM_001111018.2:c.75+196703T>C | NP_001104488.1:n.75+196703T>C |