HGVS | Genome Assembly |
---|---|
NC_000013.11:g.102845587T= , CM000675.2:g.102845587T= | GRCh38 |
NC_000013.10:g.103497937T= , CM000675.1:g.103497937T= | GRCh37 |
NC_000013.9:g.102295938T= | NCBI36 |
NG_007146.1:g.4764T= , LRG_464:g.4764T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000638434.1:c.363-8170T= (BIVM-ERCC5) | ||
ENST00000639118.1:c.363-3531T= (BIVM-ERCC5) | ||
ENST00000639132.1:c.763+5784T= (BIVM-ERCC5) | ENSP00000492684.1:n.763+5784T= | |
ENST00000639435.1:c.1450+5784T= (BIVM-ERCC5) | ENSP00000491742.1:n.1450+5784T= | |
ENST00000355739.8:c.-680T= (ERCC5) | ENSP00000347978.4:n.-680T= | |
ENST00000602836.1:c.1364+5784T= (BIVM-ERCC5) | ||
NM_001204425.1:c.1450+5784T= (BIVM-ERCC5) | NP_001191354.1:n.1450+5784T= | |
NM_001204425.2:c.1450+5784T= (BIVM-ERCC5) | NP_001191354.2:n.1450+5784T= |