Canonical Allele Identifier: CA1775343170
Gene:

Linked Data

dbSNP Id: rs1585469007
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.33808384A>T , CM000670.2:g.33808384A>T GRCh38
NC_000008.10:g.33665902A>T , CM000670.1:g.33665902A>T GRCh37
NC_000008.9:g.33785444A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949659.1:n.240+11948A>T
XR_002956701.1:n.240+11948A>T
Search 100 bp 5'
Search 100 bp 3'