Canonical Allele Identifier: CA1841175637
Gene:

Linked Data

dbSNP Id: rs1819678384
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551516C>G , CM000671.2:g.25551516C>G GRCh38
NC_000009.11:g.25551514C>G , CM000671.1:g.25551514C>G GRCh37
NC_000009.10:g.25541514C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-944G>C
XR_929525.2:n.674-944G>C
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