HGVS | Genome Assembly |
---|---|
NC_000001.11:g.111565001A>T , CM000663.2:g.111565001A>T | GRCh38 |
NC_000001.10:g.112107623A>T , CM000663.1:g.112107623A>T | GRCh37 |
NC_000001.9:g.111909146A>T | NCBI36 |
NG_032119.1:g.3975T>A , LRG_424:g.3975T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000356415.5:c.-28+22492A>T | ENSP00000348786.1:n.-28+22492A>T | |
XM_017001964.1:c.-28+22492A>T | XP_016857453.1:n.-28+22492A>T | |
NM_001370216.1:c.-28+22492A>T | NP_001357145.1:n.-28+22492A>T | |
NM_001370216.2:c.-28+22492A>T | NP_001357145.1:n.-28+22492A>T |