Canonical Allele Identifier: CA308966940

Gene: ERCC2

Linked Data

• dbSNP Id: rs372480664
• MyVariant Identifiers: chr19:g.45364165G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45364165G>A , CM000681.2:g.45364165G>A	GRCh38
NC_000019.9:g.45867423G>A , CM000681.1:g.45867423G>A	GRCh37
NC_000019.8:g.50559263G>A	NCBI36
NG_007067.2:g.11423C>T , LRG_461:g.11423C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.816-46C>T	ENSP00000375808.4:n.816-46C>T
ENST00000682414.1:c.816-46C>T	ENSP00000507019.1:n.816-46C>T
ENST00000682508.1:n.845-46C>T
ENST00000684218.1:c.*74-46C>T	ENSP00000507804.1:n.*74-46C>T
ENST00000684407.1:c.693-46C>T	ENSP00000507775.1:n.693-46C>T
ENST00000684458.1:c.816-46C>T	ENSP00000508260.1:n.816-46C>T
ENST00000391945.10:c.816-46C>T MANE Select	ENSP00000375809.4:n.816-46C>T
ENST00000586131.6:c.744-46C>T	ENSP00000464887.1:n.744-46C>T
ENST00000646507.1:n.913-46C>T
ENST00000391941.6:c.744-46C>T	ENSP00000375805.2:n.744-46C>T
ENST00000391944.7:c.582-46C>T	ENSP00000375808.3:n.582-46C>T
ENST00000391945.8:c.816-46C>T	ENSP00000375809.3:n.816-46C>T
ENST00000485403.6:c.744-46C>T	ENSP00000431229.2:n.744-46C>T
ENST00000586131.5:c.744-46C>T	ENSP00000464887.1:n.744-46C>T
ENST00000586737.5:n.453-46C>T
ENST00000591309.5:c.*74-46C>T	ENSP00000465207.1:n.*74-46C>T
NM_000400.3:c.816-46C>T , LRG_461t1:c.816-46C>T	NP_000391.1:n.816-46C>T
NM_001130867.1:c.744-46C>T	NP_001124339.1:n.744-46C>T
XM_011526611.1:c.738-46C>T	XP_011524913.1:n.738-46C>T
XR_935763.1:n.863-46C>T
XM_011526611.2:c.738-46C>T	XP_011524913.1:n.738-46C>T
XM_017026467.1:c.693-46C>T	XP_016881956.1:n.693-46C>T
XR_001753633.2:n.863-46C>T
XR_001753634.2:n.863-46C>T
NM_000400.4:c.816-46C>T MANE Select	NP_000391.1:n.816-46C>T
NM_001130867.2:c.744-46C>T	NP_001124339.1:n.744-46C>T