Canonical Allele Identifier: CA308948079

Gene: ERCC2

Linked Data

• dbSNP Id: rs890168776
• MyVariant Identifiers: chr19:g.45855210T>C (hg19) ; chr19:g.45351952T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45351952T>C , CM000681.2:g.45351952T>C	GRCh38
NC_000019.9:g.45855210T>C , CM000681.1:g.45855210T>C	GRCh37
NC_000019.8:g.50547050T>C	NCBI36
NG_007067.2:g.23636A>G , LRG_461:g.23636A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.2447A>G	ENSP00000375808.4:p.Asp816Gly
ENST00000682414.1:c.2191-231A>G	ENSP00000507019.1:n.2191-231A>G
ENST00000682508.1:n.2220-231A>G
ENST00000684218.1:c.*1449-231A>G	ENSP00000507804.1:n.*1449-231A>G
ENST00000684264.1:n.1747-231A>G
ENST00000684407.1:c.2068-231A>G	ENSP00000507775.1:n.2068-231A>G
ENST00000684458.1:c.*677-231A>G	ENSP00000508260.1:n.*677-231A>G
ENST00000684468.1:n.1903-231A>G
ENST00000391945.10:c.2191-231A>G MANE Select	ENSP00000375809.4:n.2191-231A>G
ENST00000646507.1:n.2288-231A>G
ENST00000391942.6:n.1362-231A>G
ENST00000391944.7:c.1957-231A>G	ENSP00000375808.3:n.1957-231A>G
ENST00000391945.8:c.2191-231A>G	ENSP00000375809.3:n.2191-231A>G
ENST00000588652.5:n.2279-231A>G
NM_000400.3:c.2191-231A>G , LRG_461t1:c.2191-231A>G	NP_000391.1:n.2191-231A>G
XM_011526611.1:c.2113-231A>G	XP_011524913.1:n.2113-231A>G
XM_011526611.2:c.2113-231A>G	XP_011524913.1:n.2113-231A>G
XM_017026467.1:c.2068-231A>G	XP_016881956.1:n.2068-231A>G
XR_001753633.2:n.2238-231A>G
XR_001753634.2:n.2174-231A>G
NM_000400.4:c.2191-231A>G MANE Select	NP_000391.1:n.2191-231A>G