HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104034537C= , CM000672.2:g.104034537C= | GRCh38 |
NC_000010.10:g.105794295C= , CM000672.1:g.105794295C= | GRCh37 |
NC_000010.9:g.105784285C= | NCBI36 |
NG_007069.1:g.56344G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.3520+84G= | ENSP00000358748.3:n.3520+84G= | |
ENST00000648076.2:c.3766+84G= MANE Select | ENSP00000497653.1:n.3766+84G= | |
ENST00000353479.9:c.3766+84G= | ENSP00000340937.5:n.3766+84G= | |
ENST00000369733.7:c.3520+84G= | ENSP00000358748.3:n.3520+84G= | |
NM_000494.3:c.3766+84G= | NP_000485.3:n.3766+84G= | |
NM_000494.4:c.3766+84G= MANE Select | NP_000485.3:n.3766+84G= |