HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12710332T>C , CM000686.2:g.12710332T>C | GRCh38 |
NC_000024.9:g.14822265T>C , CM000686.1:g.14822265T>C | GRCh37 |
NC_000024.8:g.13331659T>C | NCBI36 |
NG_008311.1:g.14106T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000651177.1:c.96+789T>C | ENSP00000498372.1:n.96+789T>C | |
ENST00000338981.7:c.96+789T>C MANE Select | ENSP00000342812.3:n.96+789T>C | |
ENST00000426564.6:n.108+789T>C | ||
ENST00000493168.1:n.172+789T>C | ||
NM_004654.3:c.96+789T>C | NP_004645.2:n.96+789T>C | |
XM_011531469.1:c.96+789T>C | XP_011529771.1:n.96+789T>C | |
XM_017030078.2:c.96+789T>C | XP_016885567.1:n.96+789T>C | |
NM_004654.4:c.96+789T>C MANE Select | NP_004645.2:n.96+789T>C |