HGVS | Genome Assembly |
---|---|
NC_000006.12:g.96057450A>C , CM000668.2:g.96057450A>C | GRCh38 |
NC_000006.11:g.96505326A>C , CM000668.1:g.96505326A>C | GRCh37 |
NC_000006.10:g.96612047A>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000302103.6:c.-98+41238A>C MANE Select | ENSP00000302599.4:n.-98+41238A>C | |
ENST00000302103.5:c.-98+41238A>C | ENSP00000302599.4:n.-98+41238A>C | |
NM_006581.3:c.-98+41238A>C | NP_006572.2:n.-98+41238A>C | |
XM_011535384.1:c.-98+36477A>C | XP_011533686.1:n.-98+36477A>C | |
XM_017010190.1:c.-215+41238A>C | XP_016865679.1:n.-215+41238A>C | |
XR_001744267.2:n.1808T>G | ||
NM_006581.4:c.-98+41238A>C MANE Select | NP_006572.2:n.-98+41238A>C |