HGVS | Genome Assembly |
---|---|
NC_000006.12:g.33650276C>T , CM000668.2:g.33650276C>T | GRCh38 |
NC_000006.11:g.33618053C>T , CM000668.1:g.33618053C>T | GRCh37 |
NC_000006.10:g.33726031C>T | NCBI36 |
NG_027729.1:g.33898C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000605930.3:c.161-5490C>T MANE Select | ENSP00000475177.1:n.161-5490C>T | |
ENST00000374316.9:c.161-5490C>T | ENSP00000363435.4:n.161-5490C>T | |
ENST00000605930.2:c.161-5490C>T | ENSP00000475177.1:n.161-5490C>T | |
NM_002224.3:c.161-5490C>T | NP_002215.2:n.161-5490C>T | |
XM_011514576.1:c.230-5490C>T | XP_011512878.1:n.230-5490C>T | |
XM_017010832.1:c.161-5490C>T | XP_016866321.1:n.161-5490C>T | |
NM_002224.4:c.161-5490C>T MANE Select | NP_002215.2:n.161-5490C>T |