Canonical Allele Identifier: CA1502607418
Gene:

Linked Data

dbSNP Id: rs1732906143
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748457T>G , CM000666.2:g.148748457T>G GRCh38
NC_000004.11:g.149669609T>G , CM000666.1:g.149669609T>G GRCh37
NC_000004.10:g.149889059T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118300T>G
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