Canonical Allele Identifier: CA12176998
Gene:

Linked Data

dbSNP Id: rs9378636
gnomAD v2: 6-1535895-C-T
gnomAD v3: 6-1535660-C-T
gnomAD v4: 6-1535660-C-T
MyVariant Identifiers: chr6:g.1535895C>T (hg19) chr6:g.1535660C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.1535660C>T , CM000668.2:g.1535660C>T GRCh38
NC_000006.11:g.1535895C>T , CM000668.1:g.1535895C>T GRCh37
NC_000006.10:g.1480894C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427861.2:n.234+16686G>A
XR_926380.1:n.218-2796C>T
XR_926381.1:n.1108-2796C>T
XR_926382.1:n.235-6481G>A
XR_926384.1:n.200-6481G>A
XR_001743921.1:n.235-6505G>A
XR_427861.3:n.234+16686G>A
XR_926381.2:n.1123-2796C>T
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