Canonical Allele Identifier: CA15949076

Gene: ERCC2

Linked Data

• dbSNP Id: rs50871
• gnomAD v2: 19-45862515-C-A
• gnomAD v3: 19-45359257-C-A
• gnomAD v4: 19-45359257-C-A
• MyVariant Identifiers: chr19:g.45862515C>A (hg19) ; chr19:g.45359257C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45359257C>A , CM000681.2:g.45359257C>A	GRCh38
NC_000019.9:g.45862515C>A , CM000681.1:g.45862515C>A	GRCh37
NC_000019.8:g.50554355C>A	NCBI36
NG_007067.2:g.16331G>T , LRG_461:g.16331G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.1238-1558G>T	ENSP00000375808.4:n.1238-1558G>T
ENST00000682414.1:c.1238-1558G>T	ENSP00000507019.1:n.1238-1558G>T
ENST00000682508.1:n.1267-1558G>T
ENST00000684218.1:c.*496-1558G>T	ENSP00000507804.1:n.*496-1558G>T
ENST00000684407.1:c.1115-1558G>T	ENSP00000507775.1:n.1115-1558G>T
ENST00000684458.1:c.1238-1714G>T	ENSP00000508260.1:n.1238-1714G>T
ENST00000391945.10:c.1238-1558G>T MANE Select	ENSP00000375809.4:n.1238-1558G>T
ENST00000587376.6:c.361-1558G>T
ENST00000646507.1:n.1335-1558G>T
ENST00000391941.6:c.1166-1558G>T	ENSP00000375805.2:n.1166-1558G>T
ENST00000391942.6:n.409-1558G>T
ENST00000391944.7:c.1004-1558G>T	ENSP00000375808.3:n.1004-1558G>T
ENST00000391945.8:c.1238-1558G>T	ENSP00000375809.3:n.1238-1558G>T
ENST00000485403.6:c.1166-345G>T	ENSP00000431229.2:n.1166-345G>T
ENST00000587376.5:c.361-1558G>T
NM_000400.3:c.1238-1558G>T , LRG_461t1:c.1238-1558G>T	NP_000391.1:n.1238-1558G>T
NM_001130867.1:c.1166-345G>T	NP_001124339.1:n.1166-345G>T
XM_011526611.1:c.1160-1558G>T	XP_011524913.1:n.1160-1558G>T
XR_935763.1:n.1285-1558G>T
XM_011526611.2:c.1160-1558G>T	XP_011524913.1:n.1160-1558G>T
XM_017026467.1:c.1115-1558G>T	XP_016881956.1:n.1115-1558G>T
XR_001753633.2:n.1285-1558G>T
XR_001753634.2:n.1285-1558G>T
NM_000400.4:c.1238-1558G>T MANE Select	NP_000391.1:n.1238-1558G>T
NM_001130867.2:c.1166-345G>T	NP_001124339.1:n.1166-345G>T