HGVS | Genome Assembly |
---|---|
NC_000013.11:g.102845585T= , CM000675.2:g.102845585T= | GRCh38 |
NC_000013.10:g.103497935T= , CM000675.1:g.103497935T= | GRCh37 |
NC_000013.9:g.102295936T= | NCBI36 |
NG_007146.1:g.4762T= , LRG_464:g.4762T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000638434.1:c.363-8172T= (BIVM-ERCC5) | ||
ENST00000639118.1:c.363-3533T= (BIVM-ERCC5) | ||
ENST00000639132.1:c.763+5782T= (BIVM-ERCC5) | ENSP00000492684.1:n.763+5782T= | |
ENST00000639435.1:c.1450+5782T= (BIVM-ERCC5) | ENSP00000491742.1:n.1450+5782T= | |
ENST00000355739.8:c.-682T= (ERCC5) | ENSP00000347978.4:n.-682T= | |
ENST00000602836.1:c.1364+5782T= (BIVM-ERCC5) | ||
NM_001204425.1:c.1450+5782T= (BIVM-ERCC5) | NP_001191354.1:n.1450+5782T= | |
NM_001204425.2:c.1450+5782T= (BIVM-ERCC5) | NP_001191354.2:n.1450+5782T= |