Canonical Allele Identifier: CA308974763
Gene: ERCC1 HGNC NCBI

Linked Data

dbSNP Id: rs892664237
gnomAD v3: 19-45459468-A-G
gnomAD v4: 19-45459468-A-G
MyVariant Identifiers: chr19:g.45962726A>G (hg19) chr19:g.45459468A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45459468A>G , CM000681.2:g.45459468A>G GRCh38
NC_000019.9:g.45962726A>G , CM000681.1:g.45962726A>G GRCh37
NC_000019.8:g.50654566A>G NCBI36
NG_015839.2:g.24361T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000423698.6:c.-8+19268T>C ENSP00000394875.2:n.-8+19268T>C
XM_005258636.3:c.-8+19268T>C XP_005258693.1:n.-8+19268T>C
XM_005258636.4:c.-8+19268T>C XP_005258693.1:n.-8+19268T>C
XM_017026464.1:c.-8+19268T>C XP_016881953.1:n.-8+19268T>C
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