HGVS | Genome Assembly |
---|---|
NC_000010.11:g.99851470T>C , CM000672.2:g.99851470T>C | GRCh38 |
NC_000010.10:g.101611227T>C , CM000672.1:g.101611227T>C | GRCh37 |
NC_000010.9:g.101601217T>C | NCBI36 |
NG_011798.1:g.73765T>C | |
NG_011798.2:g.73873T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647814.1:c.4509-32T>C MANE Select | ENSP00000497274.1:n.4509-32T>C | |
ENST00000648523.1:c.579-32T>C | ||
ENST00000370449.8:c.4509-32T>C | ENSP00000359478.4:n.4509-32T>C | |
NM_000392.4:c.4509-32T>C | NP_000383.1:n.4509-32T>C | |
XM_006717630.2:c.3813-32T>C | XP_006717693.1:n.3813-32T>C | |
XR_945605.1:n.4573-32T>C | ||
NM_000392.5:c.4509-32T>C MANE Select | NP_000383.2:n.4509-32T>C | |
XM_006717630.3:c.3813-32T>C | XP_006717693.1:n.3813-32T>C | |
XR_945605.3:n.4625-32T>C |