Canonical Allele Identifier: CA1771018655
Gene:

Linked Data

dbSNP Id: rs1512268
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23668950T>A , CM000670.2:g.23668950T>A GRCh38
NC_000008.10:g.23526463T>A , CM000670.1:g.23526463T>A GRCh37
NC_000008.9:g.23582408T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745840.1:n.1512T>A
XR_001745841.1:n.890T>A
XR_001745842.1:n.1312+200T>A
XR_001745843.1:n.1086T>A
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