Canonical Allele Identifier: CA206604148

Gene: ERCC6

Linked Data

• dbSNP Id: rs186324912
• gnomAD v3: 10-49492923-C-A
• gnomAD v4: 10-49492923-C-A
• MyVariant Identifiers: chr10:g.50700969C>A (hg19) ; chr10:g.49492923C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.49492923C>A , CM000672.2:g.49492923C>A	GRCh38
NC_000010.10:g.50700969C>A , CM000672.1:g.50700969C>A	GRCh37
NC_000010.9:g.50370975C>A	NCBI36
NG_009442.1:g.51179G>T , LRG_465:g.51179G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000355832.10:c.1821+194G>T MANE Select	ENSP00000348089.5:n.1821+194G>T
ENST00000681632.1:n.1899+194G>T
ENST00000681659.1:c.1662+194G>T	ENSP00000505631.1:n.1662+194G>T
ENST00000355832.9:c.1821+194G>T	ENSP00000348089.5:n.1821+194G>T
ENST00000475116.1:n.275+7615G>T
ENST00000623073.3:c.222+194G>T	ENSP00000485650.1:n.222+194G>T
ENST00000623115.3:c.-70+7615G>T	ENSP00000485321.1:n.-70+7615G>T
ENST00000623318.1:c.222+194G>T	ENSP00000485423.1:n.222+194G>T
NM_000124.3:c.1821+194G>T	NP_000115.1:n.1821+194G>T
NM_001346440.1:c.1821+194G>T	NP_001333369.1:n.1821+194G>T
NM_000124.4:c.1821+194G>T MANE Select	NP_000115.1:n.1821+194G>T
NM_001346440.2:c.1821+194G>T	NP_001333369.1:n.1821+194G>T