Canonical Allele Identifier: CA129965422
Gene:

Linked Data

dbSNP Id: rs953995181
MyVariant Identifiers: chr5:g.159007854T>C (hg19) chr5:g.159580846T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580846T>C , CM000667.2:g.159580846T>C GRCh38
NC_000005.9:g.159007854T>C , CM000667.1:g.159007854T>C GRCh37
NC_000005.8:g.158940432T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+411T>C
XR_941140.1:n.2075+411T>C
XR_941141.1:n.570+411T>C
XR_941139.2:n.2229+411T>C
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