HGVS | Genome Assembly |
---|---|
NC_000019.10:g.35842089G>A , CM000681.2:g.35842089G>A | GRCh38 |
NC_000019.9:g.36332991G>A , CM000681.1:g.36332991G>A | GRCh37 |
NC_000019.8:g.41024831G>A | NCBI36 |
NG_013356.2:g.32199C>T , LRG_693:g.32199C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378910.10:c.2663+35C>T MANE Select | ENSP00000368190.4:n.2663+35C>T | |
ENST00000353632.6:c.2663+35C>T | ENSP00000343634.5:n.2663+35C>T | |
ENST00000378910.9:c.2663+35C>T | ENSP00000368190.4:n.2663+35C>T | |
NM_004646.3:c.2663+35C>T , LRG_693t1:c.2663+35C>T | NP_004637.1:n.2663+35C>T | |
NM_004646.4:c.2663+35C>T MANE Select | NP_004637.1:n.2663+35C>T |