HGVS | Genome Assembly |
---|---|
NC_000022.11:g.37713456T>C , CM000684.2:g.37713456T>C | GRCh38 |
NC_000022.10:g.38109463T>C , CM000684.1:g.38109463T>C | GRCh37 |
NC_000022.9:g.36439409T>C | NCBI36 |
NG_012857.1:g.21469T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000644935.1:c.456+45T>C MANE Select | ENSP00000496394.1:n.456+45T>C | |
ENST00000344404.10:c.255-2307T>C | ENSP00000340312.6:n.255-2307T>C | |
ENST00000406386.7:c.456+45T>C | ENSP00000384312.3:n.456+45T>C | |
ENST00000455236.4:c.1413+45T>C | ENSP00000477208.1:n.1413+45T>C | |
ENST00000492485.5:n.391-2307T>C | ||
NM_001039141.2:c.456+45T>C | NP_001034230.1:n.456+45T>C | |
NM_001039141.3:c.456+45T>C MANE Select | NP_001034230.1:n.456+45T>C |