Canonical Allele Identifier: CA174890873
Gene:

Linked Data

dbSNP Id: rs780911625
MyVariant Identifiers: chr8:g.31034056A>G (hg19) chr8:g.31176540A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31176540A>G , CM000670.2:g.31176540A>G GRCh38
NC_000008.10:g.31034056A>G , CM000670.1:g.31034056A>G GRCh37
NC_000008.9:g.31153598A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949642.1:n.221A>G
XR_949643.1:n.87+152T>C
XR_949644.1:n.87+152T>C
XR_949645.1:n.87+152T>C
XR_949646.1:n.87+152T>C
XR_949647.1:n.700+152T>C
XR_949648.1:n.602+152T>C
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