HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104034617C>A , CM000672.2:g.104034617C>A | GRCh38 |
NC_000010.10:g.105794375C>A , CM000672.1:g.105794375C>A | GRCh37 |
NC_000010.9:g.105784365C>A | NCBI36 |
NG_007069.1:g.56264G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.3520+4G>T | ENSP00000358748.3:n.3520+4G>T | |
ENST00000648076.2:c.3766+4G>T MANE Select | ENSP00000497653.1:n.3766+4G>T | |
ENST00000353479.9:c.3766+4G>T | ENSP00000340937.5:n.3766+4G>T | |
ENST00000369733.7:c.3520+4G>T | ENSP00000358748.3:n.3520+4G>T | |
NM_000494.3:c.3766+4G>T | NP_000485.3:n.3766+4G>T | |
NM_000494.4:c.3766+4G>T MANE Select | NP_000485.3:n.3766+4G>T |