Canonical Allele Identifier: CA1979711948
Gene:

Linked Data

dbSNP Id: rs1855915056
gnomAD v4: 11-66510568-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66510568C>A , CM000673.2:g.66510568C>A GRCh38
NC_000011.9:g.66278039C>A , CM000673.1:g.66278039C>A GRCh37
NC_000011.8:g.66034615C>A NCBI36
NG_009093.1:g.4921C>A
NG_032068.1:g.35160C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000419755.3:c.159-445C>A ENSP00000398526.3:n.159-445C>A
Search 100 bp 5'
Search 100 bp 3'