HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111098306C>T , CM000667.2:g.111098306C>T | GRCh38 |
NC_000005.9:g.110434004C>T , CM000667.1:g.110434004C>T | GRCh37 |
NC_000005.8:g.110461903C>T | NCBI36 |
NG_008979.1:g.11135C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000513710.4:c.292-416C>T MANE Select | ENSP00000424628.3:n.292-416C>T | |
ENST00000504122.2:n.174-416C>T | ||
ENST00000505303.5:n.428-416C>T | ||
ENST00000506538.6:c.460-416C>T | ENSP00000423067.2:n.460-416C>T | |
ENST00000513710.3:c.292-416C>T | ENSP00000424628.3:n.292-416C>T | |
ENST00000612402.4:c.460-416C>T | ENSP00000479950.1:n.460-416C>T | |
NM_139281.2:c.460-416C>T | NP_644810.1:n.460-416C>T | |
XM_011543163.1:c.460-416C>T | XP_011541465.1:n.460-416C>T | |
NM_139281.3:c.292-416C>T MANE Select | NP_644810.2:n.292-416C>T |