Canonical Allele Identifier: CA406363755

Gene: ERCC2

Linked Data

• dbSNP Id: rs1971856905
• gnomAD v3: 19-45352767-G-C
• gnomAD v4: 19-45352767-G-C
• MyVariant Identifiers: chr19:g.45856025G>C (hg19) ; chr19:g.45352767G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352767G>C , CM000681.2:g.45352767G>C	GRCh38
NC_000019.9:g.45856025G>C , CM000681.1:g.45856025G>C	GRCh37
NC_000019.8:g.50547865G>C	NCBI36
NG_007067.2:g.22821C>G , LRG_461:g.22821C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000391944.8:c.1881C>G	ENSP00000375808.4:p.Tyr627Ter
ENST00000682414.1:c.1881C>G	ENSP00000507019.1:p.Tyr627Ter
ENST00000682508.1:n.1910C>G
ENST00000684218.1:c.*1139C>G	ENSP00000507804.1:n.*1139C>G
ENST00000684264.1:n.1437C>G
ENST00000684407.1:c.1758C>G	ENSP00000507775.1:p.Tyr586Ter
ENST00000684458.1:c.*367C>G	ENSP00000508260.1:n.*367C>G
ENST00000684468.1:n.1593C>G
ENST00000391945.10:c.1881C>G MANE Select	ENSP00000375809.4:p.Tyr627Ter
ENST00000646507.1:n.1978C>G
ENST00000391941.6:c.1809C>G	ENSP00000375805.2:p.Tyr603Ter
ENST00000391942.6:n.1052C>G
ENST00000391944.7:c.1647C>G	ENSP00000375808.3:p.Tyr549Ter
ENST00000391945.8:c.1881C>G	ENSP00000375809.3:p.Tyr627Ter
ENST00000588652.5:n.1969C>G
NM_000400.3:c.1881C>G , LRG_461t1:c.1881C>G	NP_000391.1:p.Tyr627Ter
XM_011526611.1:c.1803C>G	XP_011524913.1:p.Tyr601Ter
XM_011526611.2:c.1803C>G	XP_011524913.1:p.Tyr601Ter
XM_017026467.1:c.1758C>G	XP_016881956.1:p.Tyr586Ter
XR_001753633.2:n.1928C>G
XR_001753634.2:n.1864C>G
NM_000400.4:c.1881C>G MANE Select	NP_000391.1:p.Tyr627Ter