Canonical Allele Identifier: CA851031665
Gene:

Linked Data

dbSNP Id: rs1257176981
MyVariant Identifiers: chr8:g.33665692A>G (hg19) chr8:g.33808174A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808174A>G , CM000670.2:g.33808174A>G GRCh38
NC_000008.10:g.33665692A>G , CM000670.1:g.33665692A>G GRCh37
NC_000008.9:g.33785234A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949659.1:n.240+11738A>G
XR_002956701.1:n.240+11738A>G
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