Canonical Allele Identifier: CA133346624
Gene:

Linked Data

dbSNP Id: rs12526688
gnomAD v2: 6-465937-C-T
gnomAD v3: 6-465937-C-T
gnomAD v4: 6-465937-C-T
MyVariant Identifiers: chr6:g.465937C>T (hg19) chr6:g.465937C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465937C>T , CM000668.2:g.465937C>T GRCh38
NC_000006.11:g.465937C>T , CM000668.1:g.465937C>T GRCh37
NC_000006.10:g.410937C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926364.1:n.2714+12212C>T
XR_926365.1:n.2548+12212C>T
XR_001743914.1:n.482-9271C>T
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