HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23423942_23423943delinsTG , CM000676.2:g.23423942_23423943delinsTG | GRCh38 |
NC_000014.8:g.23893151_23893152delinsTG , CM000676.1:g.23893151_23893152delinsTG | GRCh37 |
NC_000014.7:g.22962991_22962992delinsTG | NCBI36 |
NG_007884.1:g.16719_16720delinsCA , LRG_384:g.16719_16720delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.2886_2887delinsCA MANE Select | ENSP00000347507.3:p.Ala962= | |
ENST00000355349.3:c.2886_2887delinsCA | ENSP00000347507.3:p.Ala962= | |
NM_000257.3:c.2886_2887delinsCA | NP_000248.2:p.Ala962= | |
XR_245686.3:n.2992_2993delinsCA | ||
XM_017021340.1:c.2886_2887delinsCA | XP_016876829.1:p.Ala962= | |
NM_000257.4:c.2886_2887delinsCA MANE Select | NP_000248.2:p.Ala962= |