Canonical Allele Identifier: CA708023156
Gene:

Linked Data

dbSNP Id: rs1379159846
gnomAD v3: 14-68807089-A-G
gnomAD v4: 14-68807089-A-G
MyVariant Identifiers: chr14:g.69273806A>G (hg19) chr14:g.68807089A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807089A>G , CM000676.2:g.68807089A>G GRCh38
NC_000014.8:g.69273806A>G , CM000676.1:g.69273806A>G GRCh37
NC_000014.7:g.68343559A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537441.1:c.673-435T>C XP_011535743.1:n.673-435T>C
XM_011537442.1:c.673-435T>C XP_011535744.1:n.673-435T>C
XM_011537443.1:c.673-435T>C XP_011535745.1:n.673-435T>C
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