Canonical Allele Identifier: CA2144473223
Gene:

Linked Data

dbSNP Id: rs1895390403
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807122G>T , CM000676.2:g.68807122G>T GRCh38
NC_000014.8:g.69273839G>T , CM000676.1:g.69273839G>T GRCh37
NC_000014.7:g.68343592G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537441.1:c.673-468C>A XP_011535743.1:n.673-468C>A
XM_011537442.1:c.673-468C>A XP_011535744.1:n.673-468C>A
XM_011537443.1:c.673-468C>A XP_011535745.1:n.673-468C>A
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