Canonical Allele Identifier: CA806430547
Gene:

Linked Data

dbSNP Id: rs1202972600
MyVariant Identifiers: chr5:g.159007682T>G (hg19) chr5:g.159580674T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580674T>G , CM000667.2:g.159580674T>G GRCh38
NC_000005.9:g.159007682T>G , CM000667.1:g.159007682T>G GRCh37
NC_000005.8:g.158940260T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+239T>G
XR_941140.1:n.2075+239T>G
XR_941141.1:n.570+239T>G
XR_941139.2:n.2229+239T>G
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