Canonical Allele Identifier: CA2499220245
Gene: ERCC6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1072162
ClinVar RCV Id: RCV001384813
dbSNP Id: rs2132524052

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49459235del , CM000672.2:g.49459235del GRCh38
NC_000010.10:g.50667281del , CM000672.1:g.50667281del GRCh37
NC_000010.9:g.50337287del NCBI36
NG_009442.1:g.84868del , LRG_465:g.84868del

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.4063del
ENST00000679552.1:n.2272del
ENST00000679871.1:n.1209del
ENST00000679974.1:n.1112del
ENST00000681632.1:n.5466del
ENST00000681659.1:c.3904del
ENST00000355832.9:c.4063del
ENST00000623073.3:c.*2359del
ENST00000623115.3:c.2173del
ENST00000624341.3:c.1895del
NM_000124.3:c.4063del
XR_945953.1:n.243-12330del
NM_001346440.1:c.4063del
NM_000124.4:c.4063del
NM_001346440.2:c.4063del