Canonical Allele Identifier: CA1619157023
Gene:

Linked Data

dbSNP Id: rs1761772875
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439664G>A , CM000668.2:g.31439664G>A GRCh38
NC_000006.11:g.31407441G>A , CM000668.1:g.31407441G>A GRCh37
NC_000006.10:g.31515420G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.443C>T
Search 100 bp 5'
Search 100 bp 3'