Canonical Allele Identifier: CA823881992
Gene:

Linked Data

dbSNP Id: rs1156495509
MyVariant Identifiers: chr6:g.31407764A>C (hg19) chr6:g.31439987A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439987A>C , CM000668.2:g.31439987A>C GRCh38
NC_000006.11:g.31407764A>C , CM000668.1:g.31407764A>C GRCh37
NC_000006.10:g.31515743A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926694.1:n.120T>G
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