HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31861408T>G , CM000668.2:g.31861408T>G | GRCh38 |
NC_000006.11:g.31829185T>G , CM000668.1:g.31829185T>G | GRCh37 |
NC_000006.10:g.31937164T>G | NCBI36 |
NG_008201.1:g.6525A>C | |
NG_023058.1:g.22639A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375631.5:c.395A>C MANE Select | ENSP00000364782.4:p.Asp132Ala | |
ENST00000677054.1:n.1072A>C | ||
ENST00000677512.1:n.503A>C | ||
ENST00000678869.1:n.503A>C | ||
ENST00000375631.4:c.395A>C | ENSP00000364782.4:p.Asp132Ala | |
ENST00000480384.1:n.424A>C | ||
ENST00000491768.5:c.395A>C | ENSP00000433127.1:p.Asp132Ala | |
ENST00000495807.1:n.963A>C | ||
NM_000434.3:c.395A>C | NP_000425.1:p.Asp132Ala | |
NM_000434.4:c.395A>C MANE Select | NP_000425.1:p.Asp132Ala |