Canonical Allele Identifier: CA996308536
Gene: ERCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1599878020

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45459378C>A , CM000681.2:g.45459378C>A GRCh38
NC_000019.9:g.45962636C>A , CM000681.1:g.45962636C>A GRCh37
NC_000019.8:g.50654476C>A NCBI36
NG_015839.2:g.24451G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000423698.6:c.-8+19358G>T ENSP00000394875.2:n.-8+19358G>T
XM_005258636.3:c.-8+19358G>T XP_005258693.1:n.-8+19358G>T
XM_005258636.4:c.-8+19358G>T XP_005258693.1:n.-8+19358G>T
XM_017026464.1:c.-8+19358G>T XP_016881953.1:n.-8+19358G>T