Canonical Allele Identifier: CA93117899
Gene:

Linked Data

dbSNP Id: rs1018790917
MyVariant Identifiers: chr4:g.12579741C>T (hg19) chr4:g.12578117C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578117C>T , CM000666.2:g.12578117C>T GRCh38
NC_000004.11:g.12579741C>T , CM000666.1:g.12579741C>T GRCh37
NC_000004.10:g.12188839C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31225G>A
XR_001741374.1:n.254+44538G>A
XR_925406.3:n.140+31225G>A
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