HGVS | Genome Assembly |
---|---|
NC_000002.12:g.169282972A>G , CM000664.2:g.169282972A>G | GRCh38 |
NC_000002.11:g.170139482A>G , CM000664.1:g.170139482A>G | GRCh37 |
NC_000002.10:g.169847728A>G | NCBI36 |
NG_012634.1:g.84641T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000649046.1:c.1072T>C MANE Select | ENSP00000496870.1:p.Cys358Arg | |
ENST00000263816.7:c.1072T>C | ENSP00000263816.3:p.Cys358Arg | |
ENST00000443831.1:c.1072T>C | ENSP00000409813.1:p.Cys358Arg | |
NM_004525.2:c.1072T>C | NP_004516.2:p.Cys358Arg | |
XM_011511183.1:c.1072T>C | XP_011509485.1:p.Cys358Arg | |
XM_011511185.1:c.1072T>C | XP_011509487.1:p.Cys358Arg | |
NM_004525.3:c.1072T>C MANE Select | NP_004516.2:p.Cys358Arg | |
XM_011511183.3:c.1072T>C | XP_011509485.1:p.Cys358Arg |