Canonical Allele Identifier: CA2144473220
Gene:

Linked Data

dbSNP Id: rs1895390323
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807117C>T , CM000676.2:g.68807117C>T GRCh38
NC_000014.8:g.69273834C>T , CM000676.1:g.69273834C>T GRCh37
NC_000014.7:g.68343587C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011537441.1:c.673-463G>A XP_011535743.1:n.673-463G>A
XM_011537442.1:c.673-463G>A XP_011535744.1:n.673-463G>A
XM_011537443.1:c.673-463G>A XP_011535745.1:n.673-463G>A
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