Canonical Allele Identifier: CA308951093

Gene: ERCC2

Linked Data

• dbSNP Id: rs375431433
• gnomAD v2: 19-45855973-G-A
• gnomAD v3: 19-45352715-G-A
• gnomAD v4: 19-45352715-G-A
• MyVariant Identifiers: chr19:g.45855973G>A (hg19) ; chr19:g.45352715G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45352715G>A , CM000681.2:g.45352715G>A	GRCh38
NC_000019.9:g.45855973G>A , CM000681.1:g.45855973G>A	GRCh37
NC_000019.8:g.50547813G>A	NCBI36
NG_007067.2:g.22873C>T , LRG_461:g.22873C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000391944.8:c.1902+31C>T	ENSP00000375808.4:n.1902+31C>T
ENST00000682414.1:c.1902+31C>T	ENSP00000507019.1:n.1902+31C>T
ENST00000682508.1:n.1931+31C>T
ENST00000684218.1:c.*1160+31C>T	ENSP00000507804.1:n.*1160+31C>T
ENST00000684264.1:n.1458+31C>T
ENST00000684407.1:c.1779+31C>T	ENSP00000507775.1:n.1779+31C>T
ENST00000684458.1:c.*388+31C>T	ENSP00000508260.1:n.*388+31C>T
ENST00000684468.1:n.1614+31C>T
ENST00000391945.10:c.1902+31C>T MANE Select	ENSP00000375809.4:n.1902+31C>T
ENST00000646507.1:n.1999+31C>T
ENST00000391941.6:c.1830+31C>T	ENSP00000375805.2:n.1830+31C>T
ENST00000391942.6:n.1073+31C>T
ENST00000391944.7:c.1668+31C>T	ENSP00000375808.3:n.1668+31C>T
ENST00000391945.8:c.1902+31C>T	ENSP00000375809.3:n.1902+31C>T
ENST00000588652.5:n.1990+31C>T
NM_000400.3:c.1902+31C>T , LRG_461t1:c.1902+31C>T	NP_000391.1:n.1902+31C>T
XM_011526611.1:c.1824+31C>T	XP_011524913.1:n.1824+31C>T
XM_011526611.2:c.1824+31C>T	XP_011524913.1:n.1824+31C>T
XM_017026467.1:c.1779+31C>T	XP_016881956.1:n.1779+31C>T
XR_001753633.2:n.1949+31C>T
XR_001753634.2:n.1885+31C>T
NM_000400.4:c.1902+31C>T MANE Select	NP_000391.1:n.1902+31C>T