Canonical Allele Identifier: CA1619157027
Gene:

Linked Data

dbSNP Id: rs1761773216
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439669C>T , CM000668.2:g.31439669C>T GRCh38
NC_000006.11:g.31407446C>T , CM000668.1:g.31407446C>T GRCh37
NC_000006.10:g.31515425C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_926694.1:n.438G>A
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Search 100 bp 3'