Canonical Allele Identifier: CA2706650091
Gene:

Linked Data

dbSNP Id: rs2110153065
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99474392A>T , CM000666.2:g.99474392A>T GRCh38
NC_000004.11:g.100395549A>T , CM000666.1:g.100395549A>T GRCh37
NC_000004.10:g.100614572A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000506494.1:n.242+2356T>A
Search 100 bp 5'
Search 100 bp 3'