Canonical Allele Identifier: CA2717992042
Gene:

Linked Data

dbSNP Id: rs2130730792
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269793A>G , CM000670.2:g.97269793A>G GRCh38
NC_000008.10:g.98282021A>G , CM000670.1:g.98282021A>G GRCh37
NC_000008.9:g.98351197A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149277T>C
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Search 100 bp 3'