Canonical Allele Identifier: CA1968513044
Gene:

Linked Data

dbSNP Id: rs1856778595
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506592C>T , CM000673.2:g.45506592C>T GRCh38
NC_000011.9:g.45528142C>T , CM000673.1:g.45528142C>T GRCh37
NC_000011.8:g.45484718C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16821G>A
XR_931245.3:n.566-16821G>A
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