Canonical Allele Identifier: CA1250829334
Gene:

Linked Data

dbSNP Id: rs1668655256
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722362T>A , CM000664.2:g.52722362T>A GRCh38
NC_000002.11:g.52949500T>A , CM000664.1:g.52949500T>A GRCh37
NC_000002.10:g.52803004T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.895A>T
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