Canonical Allele Identifier: CA882727758
Gene: ERCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1280300220
gnomAD v3: 19-45459455-CA-C
gnomAD v4: 19-45459455-CA-C
MyVariant Identifiers: chr19:g.45962714del (hg19) chr19:g.45459456del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45459460del , CM000681.2:g.45459460del GRCh38
NC_000019.9:g.45962718del , CM000681.1:g.45962718del GRCh37
NC_000019.8:g.50654558del NCBI36
NG_015839.2:g.24373del

Transcript Alleles

HGVS Amino-acid change
ENST00000423698.6:c.-8+19280del ENSP00000394875.2:n.-8+19280del
XM_005258636.3:c.-8+19280del XP_005258693.1:n.-8+19280del
XM_005258636.4:c.-8+19280del XP_005258693.1:n.-8+19280del
XM_017026464.1:c.-8+19280del XP_016881953.1:n.-8+19280del
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