HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19116480T>G , CM000669.2:g.19116480T>G | GRCh38 |
NC_000007.13:g.19156103T>G , CM000669.1:g.19156103T>G | GRCh37 |
NC_000007.12:g.19122628T>G | NCBI36 |
NG_008114.1:g.6193A>C | |
NG_008114.2:g.6193A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.*42+191A>C MANE Select | ENSP00000242261.5:n.*42+191A>C | |
ENST00000242261.5:c.*42+191A>C | ENSP00000242261.5:n.*42+191A>C | |
ENST00000354571.5:c.448+191A>C | ||
ENST00000443687.5:c.254+191A>C | ||
NM_000474.3:c.*42+191A>C | NP_000465.1:n.*42+191A>C | |
XM_011515496.1:c.*42+191A>C | XP_011513798.1:n.*42+191A>C | |
NR_149001.1:n.1002+191A>C | ||
NM_000474.4:c.*42+191A>C MANE Select | NP_000465.1:n.*42+191A>C | |
NR_149001.2:n.966+191A>C |