Canonical Allele Identifier: CA308974771
Gene: ERCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1052654370

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45459513T>G , CM000681.2:g.45459513T>G GRCh38
NC_000019.9:g.45962771T>G , CM000681.1:g.45962771T>G GRCh37
NC_000019.8:g.50654611T>G NCBI36
NG_015839.2:g.24316A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000423698.6:c.-8+19223A>C ENSP00000394875.2:n.-8+19223A>C
XM_005258636.3:c.-8+19223A>C XP_005258693.1:n.-8+19223A>C
XM_005258636.4:c.-8+19223A>C XP_005258693.1:n.-8+19223A>C
XM_017026464.1:c.-8+19223A>C XP_016881953.1:n.-8+19223A>C