Canonical Allele Identifier: CA2197752689
Gene:

Linked Data

dbSNP Id: rs1899530650
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.95782365G>A , CM000677.2:g.95782365G>A GRCh38
NC_000015.9:g.96325594G>A , CM000677.1:g.96325594G>A GRCh37
NC_000015.8:g.94126598G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932654.1:n.148-42824G>A
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