HGVS | Genome Assembly |
---|---|
NC_000016.10:g.2496140A= , CM000678.2:g.2496140A= | GRCh38 |
NC_000016.9:g.2546141A= , CM000678.1:g.2546141A= | GRCh37 |
NC_000016.8:g.2486142A= | NCBI36 |
NG_028170.1:g.25995A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000562105.2:c.-9A= | ENSP00000457896.2:n.-9A= | |
ENST00000567020.6:c.-9A= | ENSP00000454408.1:n.-9A= | |
ENST00000569874.2:c.-9A= | ENSP00000455005.2:n.-9A= | |
ENST00000643767.1:c.-9A= | ENSP00000494145.1:n.-9A= | |
ENST00000646147.1:c.-9A= MANE Select | ENSP00000494678.1:n.-9A= | |
ENST00000293970.9:c.-9A= | ENSP00000293970.5:n.-9A= | |
ENST00000562105.1:c.-9A= | ENSP00000457896.1:n.-9A= | |
ENST00000564543.1:c.-9A= | ENSP00000455547.1:n.-9A= | |
ENST00000567020.5:c.-9A= | ENSP00000454408.1:n.-9A= | |
ENST00000627285.1:c.-9A= | ENSP00000486121.1:n.-9A= | |
ENST00000630263.2:c.-9A= | ENSP00000486835.1:n.-9A= | |
NM_001199107.1:c.-9A= | NP_001186036.1:n.-9A= | |
NM_020705.2:c.-9A= | NP_065756.1:n.-9A= | |
XM_017023493.1:c.-9A= | XP_016878982.1:n.-9A= | |
XM_017023494.1:c.-9A= | XP_016878983.1:n.-9A= | |
XM_017023495.1:c.-9A= | XP_016878984.1:n.-9A= | |
XR_001751956.1:n.174A= | ||
NM_001199107.2:c.-9A= MANE Select | NP_001186036.1:n.-9A= | |
NM_020705.3:c.-9A= | NP_065756.1:n.-9A= |