HGVS | Genome Assembly |
---|---|
NC_000005.10:g.74685321A>G , CM000667.2:g.74685321A>G | GRCh38 |
NC_000005.9:g.73981146A>G , CM000667.1:g.73981146A>G | GRCh37 |
NC_000005.8:g.74016902A>G | NCBI36 |
NG_009770.1:g.5178A>G | |
NG_009770.2:g.50299A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261416.12:c.61A>G MANE Select | ENSP00000261416.7:p.Thr21Ala | |
ENST00000261416.11:c.61A>G | ENSP00000261416.7:p.Thr21Ala | |
ENST00000511181.5:c.-376-4007A>G | ENSP00000426285.1:n.-376-4007A>G | |
ENST00000513079.5:n.126A>G | ||
ENST00000515528.1:n.116A>G | ||
NM_000521.3:c.61A>G | NP_000512.1:p.Thr21Ala | |
NM_001292004.1:c.-376-4007A>G | NP_001278933.1:n.-376-4007A>G | |
NM_000521.4:c.61A>G MANE Select | NP_000512.2:p.Thr21Ala | |
NM_001292004.2:c.-376-4007A>G | NP_001278933.1:n.-376-4007A>G |