Canonical Allele Identifier: CA806430634
Gene:

Linked Data

dbSNP Id: rs1196852875
MyVariant Identifiers: chr5:g.159008050A>G (hg19) chr5:g.159581043A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159581043A>G , CM000667.2:g.159581043A>G GRCh38
NC_000005.9:g.159008050A>G , CM000667.1:g.159008050A>G GRCh37
NC_000005.8:g.158940628A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_941139.1:n.2075+608A>G
XR_941140.1:n.2075+608A>G
XR_941141.1:n.570+608A>G
XR_941139.2:n.2229+608A>G
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