Canonical Allele Identifier: CA2378344893
Gene:

Linked Data

dbSNP Id: rs1987464321
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.15440766A>T , CM000683.2:g.15440766A>T GRCh38
NC_000021.8:g.16813085A>T , CM000683.1:g.16813085A>T GRCh37
NC_000021.7:g.15734956A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_937593.1:n.552+460T>A
XR_001754965.2:n.468+3258T>A
XR_001754970.2:n.468+3258T>A
XR_001754971.2:n.468+3258T>A
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