Canonical Allele Identifier: CA262840974
Gene:

Linked Data

dbSNP Id: rs904089634
gnomAD v2: 14-69273923-C-T
gnomAD v3: 14-68807206-C-T
gnomAD v4: 14-68807206-C-T
COSMIC: COSN8848630 COSN15490570
MyVariant Identifiers: chr14:g.69273923C>T (hg19) chr14:g.68807206C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.68807206C>T , CM000676.2:g.68807206C>T GRCh38
NC_000014.8:g.69273923C>T , CM000676.1:g.69273923C>T GRCh37
NC_000014.7:g.68343676C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011537441.1:c.673-552G>A XP_011535743.1:n.673-552G>A
XM_011537442.1:c.673-552G>A XP_011535744.1:n.673-552G>A
XM_011537443.1:c.673-552G>A XP_011535745.1:n.673-552G>A
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