Canonical Allele Identifier: CA129965332
Gene:

Linked Data

dbSNP Id: rs902943505
gnomAD v3: 5-159580676-A-G
gnomAD v4: 5-159580676-A-G
MyVariant Identifiers: chr5:g.159007684A>G (hg19) chr5:g.159580676A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580676A>G , CM000667.2:g.159580676A>G GRCh38
NC_000005.9:g.159007684A>G , CM000667.1:g.159007684A>G GRCh37
NC_000005.8:g.158940262A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+241A>G
XR_941140.1:n.2075+241A>G
XR_941141.1:n.570+241A>G
XR_941139.2:n.2229+241A>G
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