Canonical Allele Identifier: CA1619157198
Gene:

Linked Data

dbSNP Id: rs1041645777
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31440114C>A , CM000668.2:g.31440114C>A GRCh38
NC_000006.11:g.31407891C>A , CM000668.1:g.31407891C>A GRCh37
NC_000006.10:g.31515870C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.55-62G>T
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Search 100 bp 3'