Canonical Allele Identifier: CA1775343195
Gene:

Linked Data

dbSNP Id: rs1802343487
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808420A>C , CM000670.2:g.33808420A>C GRCh38
NC_000008.10:g.33665938A>C , CM000670.1:g.33665938A>C GRCh37
NC_000008.9:g.33785480A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949659.1:n.240+11984A>C
XR_002956701.1:n.240+11984A>C
Search 100 bp 5'
Search 100 bp 3'