Canonical Allele Identifier: CA1250829272
Gene:

Linked Data

dbSNP Id: rs1668652952
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722243G>T , CM000664.2:g.52722243G>T GRCh38
NC_000002.11:g.52949381G>T , CM000664.1:g.52949381G>T GRCh37
NC_000002.10:g.52802885G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.1014C>A
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