Canonical Allele Identifier: CA127231937
Gene:

Linked Data

dbSNP Id: rs915551914
MyVariant Identifiers: chr5:g.125338430G>A (hg19) chr5:g.126002737G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.126002737G>A , CM000667.2:g.126002737G>A GRCh38
NC_000005.9:g.125338430G>A , CM000667.1:g.125338430G>A GRCh37
NC_000005.8:g.125366329G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_948737.1:n.565+3603C>T
XR_948738.1:n.497+5803C>T
Search 100 bp 5'
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