HGVS | Genome Assembly |
---|---|
NC_000002.12:g.74145290T>G , CM000664.2:g.74145290T>G | GRCh38 |
NC_000002.11:g.74372417T>G , CM000664.1:g.74372417T>G | GRCh37 |
NC_000002.10:g.74225925T>G | NCBI36 |
NG_031910.1:g.7623A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327428.10:c.68A>C MANE Select | ENSP00000331369.5:p.His23Pro | |
ENST00000295326.4:c.68A>C | ENSP00000295326.4:p.His23Pro | |
ENST00000327428.9:c.68A>C | ENSP00000331369.5:p.His23Pro | |
ENST00000469676.1:n.1091A>C | ||
ENST00000477685.5:n.219A>C | ||
ENST00000484655.1:n.2623A>C | ||
NM_001035505.1:c.68A>C | NP_001030582.1:p.His23Pro | |
NM_212552.2:c.68A>C | NP_997717.2:p.His23Pro | |
NM_212552.3:c.68A>C MANE Select | NP_997717.2:p.His23Pro | |
NM_001035505.2:c.68A>C | NP_001030582.1:p.His23Pro |