Canonical Allele Identifier: CA815488054
Gene:

Linked Data

dbSNP Id: rs1344703541
MyVariant Identifiers: chr5:g.91518801G>C (hg19) chr5:g.92222984G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222984G>C , CM000667.2:g.92222984G>C GRCh38
NC_000005.9:g.91518801G>C , CM000667.1:g.91518801G>C GRCh37
NC_000005.8:g.91554557G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18300G>C
Search 100 bp 5'
Search 100 bp 3'