Canonical Allele Identifier: CA823881976
Gene:

Linked Data

dbSNP Id: rs912802004
MyVariant Identifiers: chr6:g.31407760A>C (hg19) chr6:g.31439983A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439983A>C , CM000668.2:g.31439983A>C GRCh38
NC_000006.11:g.31407760A>C , CM000668.1:g.31407760A>C GRCh37
NC_000006.10:g.31515739A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926694.1:n.124T>G
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