HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91055342A>G , CM000674.2:g.91055342A>G | GRCh38 |
NC_000012.11:g.91449119A>G , CM000674.1:g.91449119A>G | GRCh37 |
NC_000012.10:g.89973250A>G | NCBI36 |
NG_021223.1:g.8013T>C , LRG_538:g.8013T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266719.4:c.886+54T>C MANE Select | ENSP00000266719.3:n.886+54T>C | |
ENST00000266719.3:c.886+54T>C | ENSP00000266719.3:n.886+54T>C | |
NM_007035.3:c.886+54T>C , LRG_538t1:c.886+54T>C | NP_008966.1:n.886+54T>C | |
XM_011537781.1:c.886+54T>C | XP_011536083.1:n.886+54T>C | |
NM_007035.4:c.886+54T>C MANE Select | NP_008966.1:n.886+54T>C |