Canonical Allele Identifier: CA1502607354
Gene:

Linked Data

dbSNP Id: rs1732905926
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748448A>C , CM000666.2:g.148748448A>C GRCh38
NC_000004.11:g.149669600A>C , CM000666.1:g.149669600A>C GRCh37
NC_000004.10:g.149889050A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-118309A>C
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