HGVS | Genome Assembly |
---|---|
NC_000016.10:g.28844958G>T , CM000678.2:g.28844958G>T | GRCh38 |
NC_000016.9:g.28856279G>T , CM000678.1:g.28856279G>T | GRCh37 |
NC_000016.8:g.28763780G>T | NCBI36 |
NG_008964.1:g.6451C>A | |
NG_029706.2:g.3359G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000313511.8:c.512C>A MANE Select | ENSP00000322439.3:p.Ala171Asp | |
ENST00000313511.7:c.512C>A | ENSP00000322439.3:p.Ala171Asp | |
ENST00000561644.1:n.50C>A | ||
ENST00000565012.1:c.*39C>A | ENSP00000455007.1:n.*39C>A | |
NM_003321.4:c.512C>A | NP_003312.3:p.Ala171Asp | |
XM_011545928.1:c.512C>A | XP_011544230.1:p.Ala171Asp | |
NM_001365360.1:c.512C>A | NP_001352289.1:p.Ala171Asp | |
NM_003321.5:c.512C>A MANE Select | NP_003312.3:p.Ala171Asp | |
NM_001365360.2:c.512C>A | NP_001352289.1:p.Ala171Asp |