Canonical Allele Identifier: CA1985859974
Gene:

Linked Data

dbSNP Id: rs1029879198
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851747C>T , CM000673.2:g.80851747C>T GRCh38
NC_000011.9:g.80562790C>T , CM000673.1:g.80562790C>T GRCh37
NC_000011.8:g.80240438C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_247272.2:n.124+60544G>A
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Search 100 bp 3'