Canonical Allele Identifier: CA825142482
Gene:

Linked Data

dbSNP Id: rs142141950
MyVariant Identifiers: chr6:g.465886C>A (hg19) chr6:g.465886C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.465886C>A , CM000668.2:g.465886C>A GRCh38
NC_000006.11:g.465886C>A , CM000668.1:g.465886C>A GRCh37
NC_000006.10:g.410886C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926364.1:n.2714+12161C>A
XR_926365.1:n.2548+12161C>A
XR_001743914.1:n.482-9322C>A
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