HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114716018G>A , CM000663.2:g.114716018G>A | GRCh38 |
NC_000001.10:g.115258639G>A , CM000663.1:g.115258639G>A | GRCh37 |
NC_000001.9:g.115060162G>A | NCBI36 |
NG_007572.1:g.5877C>T , LRG_92:g.5877C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.111+32C>T MANE Select | ENSP00000358548.4:n.111+32C>T | |
ENST00000369535.4:c.111+32C>T | ENSP00000358548.4:n.111+32C>T | |
NM_002524.4:c.111+32C>T | NP_002515.1:n.111+32C>T | |
NM_002524.5:c.111+32C>T MANE Select | NP_002515.1:n.111+32C>T |