HGVS | Genome Assembly |
---|---|
NC_000003.12:g.37813623C>T , CM000665.2:g.37813623C>T | GRCh38 |
NC_000003.11:g.37855114C>T , CM000665.1:g.37855114C>T | GRCh37 |
NC_000003.10:g.37830118C>T | NCBI36 |
NG_016166.1:g.366302C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264741.10:c.3010-5268C>T (ITGA9) MANE Select | ENSP00000264741.5:n.3010-5268C>T | |
ENST00000264741.9:c.3010-5268C>T (ITGA9) | ENSP00000264741.5:n.3010-5268C>T | |
ENST00000411817.2:c.110-5268C>T (ITGA9) | ||
NM_002207.2:c.3010-5268C>T (ITGA9) | NP_002198.2:n.3010-5268C>T | |
NR_110531.1:n.256+7391G>A (ITGA9-AS1) | ||
NR_110532.1:n.325+7391G>A (ITGA9-AS1) | ||
NM_002207.3:c.3010-5268C>T (ITGA9) MANE Select | NP_002198.2:n.3010-5268C>T |