Canonical Allele Identifier: CA1665449782
Gene:

Linked Data

dbSNP Id: rs1774560285
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134398884A>T , CM000668.2:g.134398884A>T GRCh38
NC_000006.11:g.134720022A>T , CM000668.1:g.134720022A>T GRCh37
NC_000006.10:g.134761715A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_428023.2:n.23+155A>T
Search 100 bp 5'
Search 100 bp 3'