Canonical Allele Identifier: CA1672979035
Gene:

Linked Data

dbSNP Id: rs1777185505
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151633495C>T , CM000668.2:g.151633495C>T GRCh38
NC_000006.11:g.151954630C>T , CM000668.1:g.151954630C>T GRCh37
NC_000006.10:g.151996323C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943115.1:n.2496+3513C>T
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