Canonical Allele Identifier: CA1674885913
Gene:

Linked Data

dbSNP Id: rs1778858841
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812674C>T , CM000668.2:g.155812674C>T GRCh38
NC_000006.11:g.156133808C>T , CM000668.1:g.156133808C>T GRCh37
NC_000006.10:g.156175500C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+19255C>T
XR_943146.1:n.645-635G>A
XR_001744423.1:n.699-635G>A
XR_001744424.1:n.79+19255C>T
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