Canonical Allele Identifier: CA308974722

Gene: ERCC1

Linked Data

• dbSNP Id: rs11083770
• MyVariant Identifiers: chr19:g.45459390G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45459390G>C , CM000681.2:g.45459390G>C	GRCh38
NC_000019.9:g.45962648G>C , CM000681.1:g.45962648G>C	GRCh37
NC_000019.8:g.50654488G>C	NCBI36
NG_015839.2:g.24439C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423698.6:c.-8+19346C>G	ENSP00000394875.2:n.-8+19346C>G
XM_005258636.3:c.-8+19346C>G	XP_005258693.1:n.-8+19346C>G
XM_005258636.4:c.-8+19346C>G	XP_005258693.1:n.-8+19346C>G
XM_017026464.1:c.-8+19346C>G	XP_016881953.1:n.-8+19346C>G