Canonical Allele Identifier: CA815487950
Gene:

Linked Data

dbSNP Id: rs1379425136
MyVariant Identifiers: chr5:g.91518547G>A (hg19) chr5:g.92222730G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222730G>A , CM000667.2:g.92222730G>A GRCh38
NC_000005.9:g.91518547G>A , CM000667.1:g.91518547G>A GRCh37
NC_000005.8:g.91554303G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18046G>A
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Search 100 bp 3'