Canonical Allele Identifier: CA11909771
Gene:

Linked Data

dbSNP Id: rs7676999
gnomAD v2: 4-116934079-C-T
gnomAD v3: 4-116012923-C-T
gnomAD v4: 4-116012923-C-T
MyVariant Identifiers: chr4:g.116934079C>T (hg19) chr4:g.116012923C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.116012923C>T , CM000666.2:g.116012923C>T GRCh38
NC_000004.11:g.116934079C>T , CM000666.1:g.116934079C>T GRCh37
NC_000004.10:g.117153528C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000508414.5:n.337-90788G>A
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