Canonical Allele Identifier: CA507822588

Gene: FOSB ERCC1

Linked Data

• dbSNP Id: rs2282695
• MyVariant Identifiers: chr19:g.45971961C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45468703C>A , CM000681.2:g.45468703C>A	GRCh38
NC_000019.9:g.45971961C>A , CM000681.1:g.45971961C>A	GRCh37
NC_000019.8:g.50663801C>A	NCBI36
NG_015839.2:g.15126G>T
NG_029675.1:g.5709C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000353609.8:c.117C>A (FOSB) MANE Select	ENSP00000245919.3:p.Ala39=
ENST00000353609.7:c.117C>A (FOSB)	ENSP00000245919.3:p.Ala39=
ENST00000417353.6:c.117C>A (FOSB)	ENSP00000407207.1:p.Ala39=
ENST00000423698.6:c.-8+10033G>T (ERCC1)	ENSP00000394875.2:n.-8+10033G>T
ENST00000443841.6:c.117C>A (FOSB)	ENSP00000414177.1:p.Ala39=
ENST00000585836.5:c.117C>A (FOSB)	ENSP00000467497.1:p.Ala39=
ENST00000590335.1:c.117C>A (FOSB)	ENSP00000465068.1:p.Ala39=
ENST00000591858.5:c.117C>A (FOSB)	ENSP00000466530.1:p.Ala39=
ENST00000592436.5:c.117C>A (FOSB)	ENSP00000465552.1:p.Ala39=
ENST00000615753.4:c.117C>A (FOSB)	ENSP00000485018.1:p.Ala39=
NM_001114171.1:c.117C>A (FOSB)	NP_001107643.1:p.Ala39=
NM_006732.2:c.117C>A (FOSB)	NP_006723.2:p.Ala39=
XM_005258636.3:c.-8+10033G>T (ERCC1)	XP_005258693.1:n.-8+10033G>T
XM_005258691.1:c.117C>A (FOSB)	XP_005258748.1:p.Ala39=
XM_005258636.4:c.-8+10033G>T (ERCC1)	XP_005258693.1:n.-8+10033G>T
XM_017026464.1:c.-8+10033G>T (ERCC1)	XP_016881953.1:n.-8+10033G>T
NM_006732.3:c.117C>A (FOSB) MANE Select	NP_006723.2:p.Ala39=
NM_001114171.2:c.117C>A (FOSB)	NP_001107643.1:p.Ala39=