Canonical Allele Identifier: CA2710978177
Gene:

Linked Data

dbSNP Id: rs2113482279
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.11943666C>A , CM000668.2:g.11943666C>A GRCh38
NC_000006.11:g.11943899C>A , CM000668.1:g.11943899C>A GRCh37
NC_000006.10:g.12051885C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001743976.1:n.348-7869C>A
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