Canonical Allele Identifier: CA928212046

Gene: ERCC6

Linked Data

• dbSNP Id: rs1851202706
• gnomAD v3: 10-49493056-C-T
• gnomAD v4: 10-49493056-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49493056C>T , CM000672.2:g.49493056C>T	GRCh38
NC_000010.10:g.50701102C>T , CM000672.1:g.50701102C>T	GRCh37
NC_000010.9:g.50371108C>T	NCBI36
NG_009442.1:g.51046G>A , LRG_465:g.51046G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.1821+61G>A MANE Select	ENSP00000348089.5:n.1821+61G>A
ENST00000681632.1:n.1899+61G>A
ENST00000681659.1:c.1662+61G>A	ENSP00000505631.1:n.1662+61G>A
ENST00000355832.9:c.1821+61G>A	ENSP00000348089.5:n.1821+61G>A
ENST00000475116.1:n.275+7482G>A
ENST00000623073.3:c.222+61G>A	ENSP00000485650.1:n.222+61G>A
ENST00000623115.3:c.-70+7482G>A	ENSP00000485321.1:n.-70+7482G>A
ENST00000623318.1:c.222+61G>A	ENSP00000485423.1:n.222+61G>A
NM_000124.3:c.1821+61G>A	NP_000115.1:n.1821+61G>A
NM_001346440.1:c.1821+61G>A	NP_001333369.1:n.1821+61G>A
NM_000124.4:c.1821+61G>A MANE Select	NP_000115.1:n.1821+61G>A
NM_001346440.2:c.1821+61G>A	NP_001333369.1:n.1821+61G>A