HGVS | Genome Assembly |
---|---|
NC_000017.11:g.42682613G>T , CM000679.2:g.42682613G>T | GRCh38 |
NC_000017.10:g.40834631G>T , CM000679.1:g.40834631G>T | GRCh37 |
NC_000017.9:g.38088157G>T | NCBI36 |
NG_042091.1:g.5000G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264638.9:c.-217G>T (CNTNAP1) MANE Select | ENSP00000264638.3:n.-217G>T | |
ENST00000264638.8:c.-217G>T (CNTNAP1) | ENSP00000264638.3:n.-217G>T | |
ENST00000591568.1:c.-643+1203C>A (CCR10) | ENSP00000467331.1:n.-643+1203C>A | |
ENST00000591765.1:c.-935C>A (CCR10) | ENSP00000468135.1:n.-935C>A | |
XM_017025238.1:c.-217G>T (CNTNAP1) | XP_016880727.1:n.-217G>T | |
XM_024451011.1:c.-217G>T (CNTNAP1) | XP_024306779.1:n.-217G>T | |
NM_003632.3:c.-217G>T (CNTNAP1) MANE Select | NP_003623.1:n.-217G>T |