HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75003522T= , CM000676.2:g.75003522T= | GRCh38 |
NC_000014.8:g.75470225T= , CM000676.1:g.75470225T= | GRCh37 |
NC_000014.7:g.74539978T= | NCBI36 |
NG_013333.1:g.5614T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266126.10:c.285-29T= MANE Select | ENSP00000266126.5:n.285-29T= | |
ENST00000266126.9:c.285-29T= | ENSP00000266126.5:n.285-29T= | |
ENST00000553401.5:c.258-29T= | ENSP00000451681.1:n.258-29T= | |
ENST00000553539.1:n.551T= | ||
ENST00000555522.1:n.343-29T= | ||
ENST00000556028.5:c.285-29T= | ENSP00000452311.1:n.285-29T= | |
NM_014239.3:c.285-29T= | NP_055054.1:n.285-29T= | |
NM_014239.4:c.285-29T= MANE Select | NP_055054.1:n.285-29T= |