Canonical Allele Identifier: CA1740470126
Gene:

Linked Data

dbSNP Id: rs1795646397
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.124306362T>G , CM000669.2:g.124306362T>G GRCh38
NC_000007.13:g.123946416T>G , CM000669.1:g.123946416T>G GRCh37
NC_000007.12:g.123733652T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002956584.1:n.73-116T>G
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