Canonical Allele Identifier: CA1908772297
Gene: ERCC6 HGNC NCBI

Linked Data

dbSNP Id: rs1851202972

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.49493065T>A , CM000672.2:g.49493065T>A GRCh38
NC_000010.10:g.50701111T>A , CM000672.1:g.50701111T>A GRCh37
NC_000010.9:g.50371117T>A NCBI36
NG_009442.1:g.51037A>T , LRG_465:g.51037A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355832.10:c.1821+52A>T MANE Select ENSP00000348089.5:n.1821+52A>T
ENST00000681632.1:n.1899+52A>T
ENST00000681659.1:c.1662+52A>T ENSP00000505631.1:n.1662+52A>T
ENST00000355832.9:c.1821+52A>T ENSP00000348089.5:n.1821+52A>T
ENST00000475116.1:n.275+7473A>T
ENST00000623073.3:c.222+52A>T ENSP00000485650.1:n.222+52A>T
ENST00000623115.3:c.-70+7473A>T ENSP00000485321.1:n.-70+7473A>T
ENST00000623318.1:c.222+52A>T ENSP00000485423.1:n.222+52A>T
NM_000124.3:c.1821+52A>T NP_000115.1:n.1821+52A>T
NM_001346440.1:c.1821+52A>T NP_001333369.1:n.1821+52A>T
NM_000124.4:c.1821+52A>T MANE Select NP_000115.1:n.1821+52A>T
NM_001346440.2:c.1821+52A>T NP_001333369.1:n.1821+52A>T