HGVS | Genome Assembly |
---|---|
NC_000014.9:g.49622012T>C , CM000676.2:g.49622012T>C | GRCh38 |
NC_000014.8:g.50088730T>C , CM000676.1:g.50088730T>C | GRCh37 |
NC_000014.7:g.49158480T>C | NCBI36 |
NG_008920.1:g.6242T>C | |
NG_033054.1:g.3620A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305386.4:c.744T>C MANE Select | ENSP00000307423.2:p.Leu248= | |
ENST00000305386.3:c.744T>C | ENSP00000307423.2:p.Leu248= | |
NM_002408.3:c.744T>C | NP_002399.1:p.Leu248= | |
NM_002408.4:c.744T>C MANE Select | NP_002399.1:p.Leu248= |