HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111098250A>C , CM000667.2:g.111098250A>C | GRCh38 |
NC_000005.9:g.110433948A>C , CM000667.1:g.110433948A>C | GRCh37 |
NC_000005.8:g.110461847A>C | NCBI36 |
NG_008979.1:g.11079A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000513710.4:c.292-472A>C MANE Select | ENSP00000424628.3:n.292-472A>C | |
ENST00000504122.2:n.174-472A>C | ||
ENST00000505303.5:n.428-472A>C | ||
ENST00000506538.6:c.460-472A>C | ENSP00000423067.2:n.460-472A>C | |
ENST00000513710.3:c.292-472A>C | ENSP00000424628.3:n.292-472A>C | |
ENST00000612402.4:c.460-472A>C | ENSP00000479950.1:n.460-472A>C | |
NM_139281.2:c.460-472A>C | NP_644810.1:n.460-472A>C | |
XM_011543163.1:c.460-472A>C | XP_011541465.1:n.460-472A>C | |
NM_139281.3:c.292-472A>C MANE Select | NP_644810.2:n.292-472A>C |