Canonical Allele Identifier: CA1205766039
Gene:

Linked Data

dbSNP Id: rs1648346422
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649465T>A , CM000663.2:g.168649465T>A GRCh38
NC_000001.10:g.168618703T>A , CM000663.1:g.168618703T>A GRCh37
NC_000001.9:g.166885327T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-8190A>T
XR_922259.2:n.332-8190A>T
Search 100 bp 5'
Search 100 bp 3'