Canonical Allele Identifier: CA1804794371
Gene:

Linked Data

dbSNP Id: rs1810400123
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269749T>G , CM000670.2:g.97269749T>G GRCh38
NC_000008.10:g.98281977T>G , CM000670.1:g.98281977T>G GRCh37
NC_000008.9:g.98351153T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149321A>C
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