HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75006171T>C , CM000676.2:g.75006171T>C | GRCh38 |
NC_000014.8:g.75472874T>C , CM000676.1:g.75472874T>C | GRCh37 |
NC_000014.7:g.74542627T>C | NCBI36 |
NG_013333.1:g.8263T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266126.10:c.693+210T>C MANE Select | ENSP00000266126.5:n.693+210T>C | |
ENST00000266126.9:c.693+210T>C | ENSP00000266126.5:n.693+210T>C | |
ENST00000553401.5:c.691+210T>C | ENSP00000451681.1:n.691+210T>C | |
ENST00000554748.2:c.57+210T>C | ENSP00000452582.2:n.57+210T>C | |
ENST00000556028.5:c.*41+210T>C | ENSP00000452311.1:n.*41+210T>C | |
NM_014239.3:c.693+210T>C | NP_055054.1:n.693+210T>C | |
NM_014239.4:c.693+210T>C MANE Select | NP_055054.1:n.693+210T>C |