Canonical Allele Identifier: CA1804794468
Gene:

Linked Data

dbSNP Id: rs1810401436
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269807A>T , CM000670.2:g.97269807A>T GRCh38
NC_000008.10:g.98282035A>T , CM000670.1:g.98282035A>T GRCh37
NC_000008.9:g.98351211A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149263T>A
Search 100 bp 5'
Search 100 bp 3'