Canonical Allele Identifier: CA683994889
Gene:

Linked Data

dbSNP Id: rs1219783835
MyVariant Identifiers: chr12:g.115836533C>T (hg19) chr12:g.115398728C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.115398728C>T , CM000674.2:g.115398728C>T GRCh38
NC_000012.11:g.115836533C>T , CM000674.1:g.115836533C>T GRCh37
NC_000012.10:g.114320916C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945389.1:n.697+8367G>A
XR_945389.2:n.701+8367G>A
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