Canonical Allele Identifier: CA815487959
Gene:

Linked Data

dbSNP Id: rs1454737059
MyVariant Identifiers: chr5:g.91518563G>C (hg19) chr5:g.92222746G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222746G>C , CM000667.2:g.92222746G>C GRCh38
NC_000005.9:g.91518563G>C , CM000667.1:g.91518563G>C GRCh37
NC_000005.8:g.91554319G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18062G>C
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Search 100 bp 3'