Canonical Allele Identifier: CA122896053
Gene:

Linked Data

dbSNP Id: rs1037260269
MyVariant Identifiers: chr5:g.91518676A>C (hg19) chr5:g.92222859A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.92222859A>C , CM000667.2:g.92222859A>C GRCh38
NC_000005.9:g.91518676A>C , CM000667.1:g.91518676A>C GRCh37
NC_000005.8:g.91554432A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948565.1:n.394+18175A>C
Search 100 bp 5'
Search 100 bp 3'