Canonical Allele Identifier: CA692802483
Gene:

Linked Data

dbSNP Id: rs1489301222
MyVariant Identifiers: chr12:g.85345678A>G (hg19) chr12:g.84951899A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84951899A>G , CM000674.2:g.84951899A>G GRCh38
NC_000012.11:g.85345678A>G , CM000674.1:g.85345678A>G GRCh37
NC_000012.10:g.83869809A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945152.1:n.316+30585A>G
XR_945153.1:n.301+13435A>G
XR_945154.1:n.174+37037A>G
XR_945155.1:n.330+30585A>G
XR_945152.2:n.316+30585A>G
XR_945154.2:n.174+37037A>G
XR_945155.2:n.888+30585A>G
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