Canonical Allele Identifier: CA1438624519
Gene:

Linked Data

dbSNP Id: rs1713320350
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.11501959A>G , CM000666.2:g.11501959A>G GRCh38
NC_000004.11:g.11503583A>G , CM000666.1:g.11503583A>G GRCh37
NC_000004.10:g.11112681A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741361.1:n.950+19113A>G
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